Recalls & alerts

602 alerts recorded, refreshed every six hours. Filter by source or category.

• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN HEART CDS983348AA CDS983348AB

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators (OPEN HEART CDS983348AA and CDS983348AB) are affected. The applicator packaging may have an open or incomplete seal, exposing patients to risk of skin, soft tissue, or systemic infection. Consumers should stop using affected kits and contact Medline Industries for instructions.

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• openFDA · September 9, 2026Moderate risk

  Baxter Healthcare Corporation : Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS

  Baxter Healthcare Corporation is recalling its Novum IQ Syringe Pump, model 40800BAXUS. A software issue during multi-syringe infusion can cause incorrect delivery when a syringe is replaced, posing a risk to patients. Consumers should contact Baxter Healthcare Corporation for instructions.

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• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F

  Medline Industries, LP is recalling two Convenience Kits: LABOR CDS (CDS981762B) and VAG DELIVERY ADMISSION BAG (DYKA1054F). The kits contain applicators with packaging that may lose sterility, exposing patients and users to microbial contamination that could cause infection. Consumers should stop using the affected kits and follow the recall instructions.

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• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT PREOP KIT DYKS1583A

  Medline Industries is recalling its Convenience Kits containing BD ChloraPrep Clear 1mL Applicators, specifically the Cataract Preop Kit DYKS1583A. The applicator packaging may have an open or incomplete seal, exposing patients to contamination that could cause skin, soft tissue, or systemic infections. Consumers should stop using affected kits and contact Medline or their healthcare provider for instructions.

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• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits: 1) ULTRASOUND BREAST PACK, Model Number: DYNJ63375C

  Medline Industries is recalling its Medline Convenience Kit ULTRASOUND BREAST PACK, model DYNJ63375C. The kits contain applicators with a potential sterility breach, exposing patients and users to microbial contamination and possible infection. The recall is voluntary and firm-initiated, with no specific consumer action listed in the notice.

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• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits: 1) DYKM1414, Catalog Number: DYKM1414; 2) DYKM1414, Catalog Number: DYKM1414; 3) DYNDH1462A, Catalog Number: DYNDH1462A; 4)…

  Medline Convenience Kits with catalog numbers DYKM1414, DYNDH1462A, DYNJ38145F, and DYNJ63199A are affected. The kits contain applicators with a potential breach of sterility, exposing patients and users to microbial contamination that may cause infection. Consumers should stop using the affected kits and contact Medline Industries for instructions.

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• openFDA · September 9, 2026Moderate risk

  Fresenius Medical Care Renal Therapies Group, LLC : GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B; 0FD3251-3B; Dry Acid Concentrate for Bicarbonate Hemodialysis

  Fresenius Medical Care Renal Therapies Group is recalling its GRANUFLO Dry Acid Concentrate, product numbers 0FD2251-3B and 0FD3251-3B, used for bicarbonate hemodialysis. The product may have blue-green discoloration, posing a potential hazard to patients undergoing dialysis. Consumers should check their product numbers and contact Fresenius Medical Care for instructions.

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• openFDA · September 9, 2026Moderate risk

  Medos International Sarl : Velys Enabling Tech Robotic-Assist Station REF: 451611001

  Medos International Sarl is recalling the Velys Enabling Tech Robotic-Assist Station, model REF 451611001. A software issue can cause unintended movement of the robotic arm during surgery, exposing patients to injury. Consumers should stop using the device and contact Medos International for instructions.

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• openFDA · September 9, 2026Moderate risk

  Philips North America Llc : Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 728324, Ingenuity Core 128 Elite Brazil 728325. Software 4.4.10.x

  Philips is recalling certain Ingenuity CT systems with software version 4.4.10.x, including specific product codes. The systems may deliver unintended radiation, which could affect patients during scans. Patients should contact their healthcare provider or Philips for further instructions.

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• openFDA · September 9, 2026Moderate risk

  Fresenius Medical Care Renal Therapies Group, LLC : 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6

  The recall affects Fresenius Medical Care Renal Therapies Group's 5008X Standard HD Pre-Flush Standard Blood Tubing Set, part number 03-5110-6. A blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment can cause blood loss and hypovolemia during treatment. Consumers should consult the FDA recall notice for instructions from the firm's voluntary recall.

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• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE DYNDH1866 BLOOD…

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators are recalled. The applicator packaging may have an open or incomplete seal, risking contamination and infection for patients. Consumers should stop using affected kits and contact Medline for return or replacement.

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• openFDA · September 9, 2026Moderate risk

  AVID Medical, Inc. : Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit) ACEN89-02; 3) BACK PACK, Model/Item…

  AVID Medical, Inc. is recalling Halyard medical convenience kits for ENT, back, spine, nasal, and other procedures. The kits contain Ritmed Neurological Sponges with potentially variable endotoxin levels, exposing patients to risk. Consumers should stop using the affected kits and contact AVID Medical for instructions.

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• openFDA · September 9, 2026Moderate risk

  Philips North America Llc : Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades Product Code: 728232. Software 4.1.10.x

  Philips Brilliance CT 64 systems with software 4.1.10.x are affected. An unintended radiation issue could affect equipment performance, exposing patients to risk. Consumers should follow the FDA recall notice for guidance.

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• openFDA · September 9, 2026Moderate risk

  Boston Scientific Corporation : LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8)

  Boston Scientific is recalling its LUX-Dx, LUX-Dx II, and LUX-Dx II+ Insertable Cardiac Monitor System server software, model 7260, all versions. The software may delay AF Burden Alert notifications, which could delay clinical evaluation or treatment for patients with these monitors. Patients should contact their healthcare provider to discuss the potential delay and any needed follow-up.

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• openFDA · September 9, 2026Moderate risk

  Cardinal Health 200, LLC : Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number: PWV2MF01D

  Cardinal Health is recalling Presource Packs containing CliniClean Pericare Wipes inside BD Urinary Catheter Trays, catalog PWV2MF01D. The wipes may be contaminated with manufacturing lubricant, causing skin irritation, redness, or mild inflammation in patients. Consumers should stop using the affected packs and contact Cardinal Health for return and replacement instructions.

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• openFDA · September 9, 2026Moderate risk

  Johnson & Johnson Surgical Vision, Inc. : HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF: 10301012 (EU); HEALON DUET PRO II, REF:…

  Johnson & Johnson Surgical Vision is recalling HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products used in cataract surgery. Forcing the cannula during insertion can cause corneal abrasion, iris trauma, or detachment of Descemet's membrane in patients. Consumers should follow the updated surgical instructions and withdraw and reassess the cannula if resistance is met, never forcing it.

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• openFDA · September 9, 2026Moderate risk

  Cardinal Health 200, LLC : Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM3; 2) KIT, ROBOTIC HYST ,…

  Cardinal Health is recalling Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays, including robotic hysterectomy and C-section kits. The wipes may be contaminated with manufacturing lubricant, causing skin irritation, redness, or mild inflammation in patients. Consumers should stop using the affected trays and contact Cardinal Health for instructions.

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• openFDA · September 9, 2026Moderate risk

  Fresenius Medical Care Renal Therapies Group, LLC : 5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8

  The recall affects Fresenius Medical Care's 5008X HD/HDF with Twister Blood Tubing Set, part number 03-5350-8. A blood leak may occur at the connection between the Arterial Alpha Clip and the main line or pump segment, exposing patients to blood loss and hypovolemia during treatment. Consumers should follow the firm's voluntary recall instructions for this product.

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• openFDA · September 9, 2026Moderate risk

  Cardinal Health 200, LLC : Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD; 2) KIT, GYN ROBOT…

  Cardinal Health 200, LLC is recalling Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays, listed under multiple catalog numbers. The wipes may be contaminated with manufacturing lubricant, causing localized skin irritation, erythema, or mild inflammation in patients. Consumers should check the recalled catalog numbers and contact Cardinal Health for return or replacement instructions.

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• openFDA · September 9, 2026Moderate risk

  Cardinal Health 200, LLC : Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) PBCGLVBLI, Catalog Number: KIT, BLO LAVH ; 2) PB15HYFCY, Catalog…

  Cardinal Health 200, LLC is recalling Presource Packs containing CliniClean Pericare Wipes inside BD Urinary Catheter Trays. The wipes may be contaminated with a lubricant, causing skin irritation, redness, or mild inflammation in patients. Consumers should stop using the affected wipes and contact Cardinal Health for instructions.

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• openFDA · September 9, 2026Moderate risk

  Diagnostica Stago, Inc. : STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor deficiency test

  Diagnostica Stago, Inc. is recalling STA Staclot Protein S reagent, catalog number 00746, lot 273074. The reagent shows a positive drift in quality control values within its stated 4-hour onboard stability period, which could affect test results for patients. Consumers should stop using the affected lot and contact Diagnostica Stago for instructions.

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• openFDA · September 9, 2026Moderate risk

  AVID Medical, Inc. : Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960, Model/Item Number (kit)…

  AVID Medical is recalling Halyard medical convenience kits, including A-P, posterior, aneurysm, spine, cervical, and crani packs. The kits contain Medicom neurological sponges with potentially variable endotoxin levels, posing a risk of fever or inflammatory reactions to patients. Consumers should stop using the recalled kits and contact AVID Medical for return or replacement instructions.

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• openFDA · September 9, 2026Moderate risk

  Medline Industries, LP : Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A

  Medline Industries, LP is recalling two Convenience Kits: Blood Culture Tray Pediatric (DYNDH1193) and Blood Culture Kit 2 w/Connect (DYNDH1487A). The kits contain applicators with a potential sterility breach due to wrinkles in the paper lidding, exposing patients and users to microbial contamination. Consumers should check whether their kit matches the recalled model numbers.

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• openFDA · September 2, 2026Moderate risk

  American Contract Systems Inc : American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP

  American Contract Systems Inc is recalling its Convenience Kits, CV B PACK, model TNCB10AP. The kits contain Medline red rubber intermittent catheters that failed performance specifications, posing a risk to patients using them. Consumers should stop using the recalled kits and contact American Contract Systems for return and replacement instructions.

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• openFDA · September 2, 2026Moderate risk

  GE Medical Systems Information Technologies Inc : PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209

  GE Medical Systems Information Technologies Inc is recalling Portrait Core Services Software V1.1, Ref# 5700209. The software may cause loss of patient monitoring at the Hub and Central Viewer and reset alarm settings to factory defaults, exposing patients to missed alarms. Consumers should contact GE Medical Systems for instructions or follow the recall notice.

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• openFDA · September 2, 2026Moderate risk

  American Contract Systems Inc : American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM

  The recall affects American Contract System Convenience Kit, CV B PACK, model TNCB10AM, which includes Medline Red Rubber Intermittent Catheters. The hazard is that the catheters failed performance specifications, posing a risk to patients using them. Consumers should stop using the kits and contact American Contract Systems or Medline for instructions.

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• openFDA · September 2, 2026Moderate risk

  Henry Schein Inc. : Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594, Mfr Product Code 1840; Lots 2529604, 2538147, 2608145 2)…

  Henry Schein Inc. is recalling Grandio Universal Nano-Hybrid Restorative Material capsules in specific lots. The affected capsules have incorrect packaging and instructions for use, posing a risk to dental professionals and patients who may use them improperly. Consumers should stop using the recalled lots and contact Henry Schein for return instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) LAVH, Medline Kit SKU CDS982273U; 2) GYN ABDOMINAL CDS, Medline Kit SKU CDS982654L; 3) GYN LAP HYSTERECTOMY CDS,…

  Medline Industries convenience kits with SKUs CDS982273U, CDS982654L, CDS982662Q, DYNJ54382F, and DYNJ903467L are affected. The kits contain a potentially contaminated component, exposing users to risk. Consumers should follow the recall instructions from Medline Industries.

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• openFDA · September 2, 2026Moderate risk

  Healthmark Industries Co., Inc. : healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001

  Healthmark Industries is recalling its ProChek-W Protein Test for Robotic Arms and ProChek-Semi Quantitative Protein Test, model PT-SQ-001. The tests were made with an expired ingredient, which can cause false negative or positive results, affecting users worldwide. Consumers should stop using the affected tests and follow the firm's recall instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS, Medline Kit SKU DYNJ9425991S

  Medline convenience kits labeled as MAJOR HEAD AND NECK PPS, Medline Kit SKU DYNJ9425991S are affected. The kits contain a potentially contaminated component, exposing users to risk. Consumers should follow the recall instructions from Medline.

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• openFDA · September 2, 2026Moderate risk

  Philips Healthcare (Suzhou) Co., Ltd. : Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.

  Philips Healthcare (Suzhou) Co., Ltd. is recalling the Philips Incisive CT with software V4.5 and V5.0, product codes 728143 and 728144. The device may fail to trigger a clinical scan during bolus tracking, affecting patients undergoing CT imaging. Consumers should contact their healthcare provider or Philips for guidance on affected scans.

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• openFDA · September 2, 2026Moderate risk

  FUJIFILM Healthcare Americas Corporation : FUJIFILM Synapse PACS software v7.4.310; radiological image processing system

  FUJIFILM Synapse PACS software version 7.4.310, a radiological image processing system, is affected by a recall. The software may produce inaccurate ruler measurements, exposing patients and healthcare providers to potential misdiagnosis or incorrect treatment decisions. Users should stop using the affected version and contact FUJIFILM Healthcare Americas Corporation for instructions and a software update.

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• openFDA · September 2, 2026Moderate risk

  American Contract Systems Inc : American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN

  American Contract Systems Inc is recalling its Convenience Kit, CV B PACK, model TNCB10AN, which includes Medline Red Rubber Intermittent Catheters. The catheters may not meet performance specifications, posing a risk to patients who use them in the states of Iowa and Ohio. Consumers should stop using the recalled kits and contact American Contract Systems for a refund or replacement.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline medical convenience kits, labeled as: 1) LAMINECTOMY PACK, Medline Kit SKU DYNJT6548; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ44504G; 3) NEURO SPINE…

  Medline Industries is recalling specific Medline medical convenience kits, including laminectomy, ortho spine, neuro spine, and craniotomy packs. The kits contain Pilling Wecksorb Neurosponges with potentially unsafe levels of endotoxin, posing a risk to patients during surgery. Consumers should check the recall notice for affected lots and follow Medline's instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline medical convenience kits, labeled as: 1) CRANIOTOMY PACK, Medline Kit SKU DYNJT6545; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ88056A; 3) ENT SINUS…

  Medline Industries is recalling certain medical convenience kits labeled as Craniotomy Pack, Ortho Spine Pack, ENT Sinus Pack, and Thyroid ENT. The kits contain neurosponges with potentially unsafe endotoxin levels, posing a risk to patients undergoing surgery. Consumers should stop using affected kits, check the lot numbers, and contact Medline for instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) OPEN HEART PACK, Medline Kit SKU CDS840393P; 2) OPEN HEART PACK, Medline Kit SKU CDS840393Q; 3) OPEN HEART PROCEDURE,…

  Medline Industries is recalling convenience kits labeled for open heart, closed heart, valve, femoral, and endoscopic procedures. The kits contain a potentially contaminated component, exposing patients to risk during surgery. Consumers should check the listed SKUs and follow the firm's recall instructions.

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• openFDA · September 2, 2026Moderate risk

  AVID Medical, Inc. : Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  AVID Medical is recalling Halyard TOTAL JOINT kits, model MSBM036-03. The kit's labeling fails to identify that the statlock component contains natural rubber latex, posing a risk to people with latex allergy. Consumers should stop using the affected kits and contact AVID Medical for instructions.

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• openFDA · September 2, 2026Moderate risk

  Midmark Corporation : Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to…

  Midmark Corporation is recalling its IQecg Digital ECG models 4-000-0061 and 4-000-0062 with software plugin versions v10 up to before v10.1.0.18. A communication anomaly can produce incorrect ECG waveforms and inaccurate beats-per-minute readings, exposing patients to misdiagnosis. Consumers should contact Midmark or their healthcare provider to obtain the software update.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) GYN ROBOTIC CDS, Medline Kit SKU CDS982888Q; 2) GYN ROBOTIC ADD ON PACK, Medline Kit SKU DYNJ43837D; 3) OH GYN/LAP…

  Medline Industries is recalling 16 convenience kits, including GYN ROBOTIC CDS and other gynecologic and laparoscopic packs, with specific SKU numbers. The kits contain a potentially contaminated component, which puts patients at risk. Consumers should check their kits against the listed SKUs and follow the recall instructions.

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• openFDA · September 2, 2026Moderate risk

  Healthmark Industries Co., Inc. : healthmark ProChek-II, Model Number PT-313, PT-201-12

  Healthmark Industries is recalling its ProChek-II tests, models PT-313 and PT-201-12. The tests were made with an expired ingredient, which can cause false negative or positive results for users worldwide. Consumers should stop using the affected tests and contact Healthmark Industries for instructions.

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• openFDA · September 2, 2026Moderate risk

  ConMed Corporation : CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures…

  The recall affects the CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver, REF# CFBC-5502B, distributed nationwide in Texas. The suture anchor may contain an incorrect patient implant card, leading to wrong device identification and traceability for patients. Consumers should contact ConMed Corporation for instructions.

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• openFDA · September 2, 2026Moderate risk

  AVID Medical, Inc. : Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  AVID Medical is recalling Halyard TOTAL JOINT Model MSBM036-03 medical kits distributed in Mississippi and Texas. The kit's labeling fails to identify that the statlock component contains natural rubber latex, posing a risk to people with latex allergy. Consumers should contact AVID Medical to return the affected kits.

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• openFDA · September 2, 2026Moderate risk

  GE Medical Systems Information Technologies Inc : FRU (Field replaceable unit), PORTRAIT CORE SERVICES SW RELOAD V1.1, Ref# 5700225

  GE Medical Systems Information Technologies Inc. is recalling the FRU (Field replaceable unit), Portrait Core Services SW Reload V1.1, Ref# 5700225. The software issue may cause loss of patient monitoring at the Hub and Central Viewer and reset alarm settings to factory defaults, affecting patients in the US and several other countries. Consumers should contact GE Medical Systems Information Technologies Inc. for instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) FEMORAL PACK, Medline Kit SKU DYNJ909393A; 2) FEVAR, Medline Kit SKU DYNJ910295D.

  Medline Industries is recalling its convenience kits labeled FEMORAL PACK (SKU DYNJ909393A) and FEVAR (SKU DYNJ910295D). The kits contain a component recalled by its manufacturer due to potential contamination, posing a risk to patients. Consumers should stop using the affected kits and contact Medline for instructions.

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• openFDA · September 2, 2026Moderate risk

  AVID Medical, Inc. : Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  AVID Medical is recalling the Halyard TOTAL JOINT kit, model MSBM036-03. The kit's labeling fails to identify that the statlock component contains natural rubber latex, posing a risk to people with latex allergy. Consumers should stop using the kit and contact AVID Medical for return or replacement instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product Number/SKU HUD78001KIT (Teleflex Product…

  Medline Industries is recalling multiple Medline Hudson RCI neonatal and infant heated wire breathing circuits, including SKUs HUD78001KIT through HUD88017KIT. The heated wire connector may discolor, melt, smoke, or burn, which can cause airway obstruction, breathing distress, and other serious risks to infants. Consumers should stop using the affected circuits and contact Medline Industries for return and replacement instructions.

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• openFDA · September 2, 2026Moderate risk

  AVID Medical, Inc. : Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  AVID Medical is recalling the Halyard TOTAL JOINT kit, model MSBM036-03. The kit's labeling does not warn that the statlock component contains natural rubber latex, posing a risk to people with latex allergies. Consumers should stop using the recalled kit and contact AVID Medical for return or replacement instructions.

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• openFDA · September 2, 2026Moderate risk

  Henry Schein Inc. : Structur 2 SC Temporary Resin Cartridge Refill 75Gm, Product Codes: 1) 114-3933, Mfr Product Code 1479; Lots 2536179, 2606429 2) 114-3934, Mfr Product Code…

  Henry Schein Inc. is recalling Structur 2 SC Temporary Resin Cartridge Refill 75Gm in specific lots. The affected cartridges were distributed with incorrect packaging and instructions for use, which could lead to improper use by dental professionals. Consumers should stop using the recalled lots and contact Henry Schein for return or replacement.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU DYNJ32770V; 3) NEURO BUNDLE-LF, Medline…

  Medline medical convenience kits, including Neuro CDS, Neuro Pack, and other labeled kits, are affected. The kits contain neurosponges with potentially unsafe endotoxin levels, posing a risk to patients during surgical procedures. Consumers should stop using the recalled kits and contact Medline for instructions.

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• openFDA · September 2, 2026Moderate risk

  Midmark Corporation : Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.

  The recall affects Midmark Digital ECG HD+12 and HD+15 devices, model 4-000-0080, with Midmark IQecg plugin versions from v10 up to before v10.1.0.18. A communication anomaly can produce incorrect ECG waveforms and inaccurate beats-per-minute readings, exposing patients to misdiagnosis. Consumers should follow the voluntary recall instructions from Midmark.

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Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.