Recalls & alerts

1278 alerts recorded, refreshed every six hours. Filter by source or category.

• 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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• openFDA · September 2, 2026Moderate risk

  Hollister Ulc : Onli 17cm Hydrophilic Urethral Intermittent Catheter, labeled as: 1) 82081 Ch08-17 Onli Hydrophilic Urethral Intermittent Catheter, SKU/REF 82081; 2) 82101…

  Hollister is recalling its Onli 17cm Hydrophilic Urethral Intermittent Catheter, including multiple SKU/REF numbers. A manufacturing defect can cause a protrusion that may lead to genitourinary trauma or bleeding in users. Consumers should stop using the affected catheters and follow the recall instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330

  Medline Industries is recalling its medical convenience kit labeled as TRACH TUBE KIT, SKU DYKM2330. The hazard is a component labeling discrepancy, affecting users of the kit. Consumers should consult the FDA recall notice for the required action.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) MAJOR GYN PACK, Medline Kit SKU DYNJG001030C; 2) GYN LITHOTOMY PACK, Medline Kit SKU DYNJT8166; 3) OPEN HEART PACK,…

  Medline Industries is recalling multiple convenience kits, including Major Gyn Pack, Open Heart Pack, and others, with specific SKUs. The kits contain a potentially contaminated component, exposing patients and users to risk. Consumers should refer to the FDA recall notice for instructions.

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• openFDA · September 2, 2026Moderate risk

  GE Medical Systems Information Technologies Inc : PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592

  GE Medical Systems Information Technologies Inc is recalling PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592. The software issue may cause loss of patient monitoring and reset alarm settings, putting patients at risk. Consumers should contact the firm for instructions or updates.

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• openFDA · September 2, 2026Moderate risk

  GE Medical Systems Information Technologies Inc : PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353

  GE Medical Systems' Portrait Core Services Software V1.0.5, Ref# 5697353, is recalled. The hazard is loss of patient monitoring and reset alarm settings, exposing patients in the US and other listed countries. Users should contact GE Medical Systems for instructions.

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• openFDA · September 2, 2026Moderate risk

  American Contract Systems Inc : American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H

  American Contract Systems Inc is recalling its Convenience Kit, D & C PACK, model LLPD90H. The kit contains Medline red rubber catheters that failed performance specifications, posing a risk to patients using them. Consumers should stop using the affected kits and contact American Contract Systems Inc for instructions.

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• openFDA · September 2, 2026Moderate risk

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

  AVID Medical, Inc. is recalling Halyard TOTAL JOINT Model/Catalog Number MSBM036-03 medical kits. 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 recalled kit and contact AVID Medical, Inc. for instructions.

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• openFDA · September 2, 2026Moderate risk

  AVID Medical, Inc. : Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: SAMM064-27

  The recall affects Halyard DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK, model SAMM064-27. The kit's labeling fails to identify that the statlock component contains natural rubber latex, which can harm people with latex allergy. Consumers should contact AVID Medical for instructions on returning or replacing the affected kit.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M

  Medline Industries is recalling its convenience kits labeled LTP CDS-LF, SKU CDS980375M, distributed nationwide in several states. The kits contain a potentially contaminated component, exposing users to a health risk. Consumers should stop using the recalled kits 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, Inc. is recalling Halyard TOTAL JOINT Model/Catalog Number MSBM036-03 medical kits. The labeling fails to identify that the statlock component contains natural rubber latex, posing a risk to people with latex allergies. Consumers should follow the recall instructions from AVID Medical.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline Hudson RCI, DBD-CIRCUIT,VENT,INSPIRATORY,HEATED,NEO, Medline Product Number/SKU HUD78019 (Teleflex Product Number/SKU 780-19); breathing circuit

  Medline Hudson RCI breathing circuit, product number HUD78019 (Teleflex 780-19), is affected. The heated wire connector may overheat, causing smoke or melting, which can lead to airway obstruction and respiratory distress in infants. Consumers should contact Medline Industries for further instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit SKU DYNJ40154D; 3) ENT PACK, Medline Kit…

  Medline is recalling certain medical convenience kits labeled as sinus, ENT, head and neck, and transsphenoidal packs with specific SKU numbers. The kits contain neurosponges with potentially unsafe endotoxin levels, posing a risk to patients during procedures. Consumers should stop using the recalled kits and contact Medline for instructions on returning them.

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• openFDA · September 2, 2026Moderate risk

  Canon Medical System, USA, INC. : Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography…

  Canon Medical Systems is recalling Alphenix models INFX-8000C, INFX-8000F, and INFX-8000V digital radiography/fluoroscopy systems. The ceiling movement gear screws may become loose, posing a risk to patients and staff during procedures. Consumers should contact Canon Medical Systems for instructions on inspection and repair.

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• openFDA · September 2, 2026Moderate risk

  Merge Healthcare, Inc. : Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation

  Merge Healthcare, Inc. is recalling Merge PACS and Merge OrthoPACS medical imaging diagnostic workstations. The software may display inaccurate measurements, posing a risk to patients whose diagnoses rely on these images. Consumers should contact Merge Healthcare or their healthcare provider for instructions on updating or correcting the software.

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• openFDA · September 2, 2026Moderate risk

  Fresenius Medical Care Renal Therapies Group, LLC : Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.

  Fresenius Medical Care is recalling its 2008T BlueStar Hemodialysis Machine, model numbers 191126 and 191130. The machine may trigger flow, no-water, or temperature alarms, exposing patients to treatment interruptions or harm. Consumers should follow the recall instructions and contact Fresenius Medical Care for guidance.

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• openFDA · September 2, 2026Moderate risk

  Olympus Corporation of the Americas : POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories

  Olympus Corporation is recalling its POWERSEAL 5 mm 23 cm Curved Jaw Sealer & Divider electrosurgical device. The outer shelf box may be incorrectly labeled as a 37-cm device, posing a risk to patients and healthcare providers. Consumers should contact Olympus Corporation to return the affected device or receive instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755; 3) AHR C-SECTION KIT, Medline Kit SKU…

  Medline Industries is recalling C-section convenience kits with SKUs DYNJ904612L, DYNJ911755, and DYNJ912014. Users of these kits may be exposed to a potentially contaminated component. Consumers should stop using the affected kits and follow the recall instructions.

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• openFDA · September 2, 2026Moderate risk

  IMRIS Imaging Inc : ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600

  IMRIS Imaging Inc is recalling its ORT300 operating room table, including Modular Table Main Unit Assy part numbers 114093-000 and 114093-600. The linear actuator and rotational lock can fail, causing unintended table movement and possible injury to patients during procedures. Consumers should contact IMRIS Imaging Inc for instructions on returning or servicing the affected tables.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/SKU 780-07);…

  Medline Industries is recalling Hudson RCI heated wire breathing circuits used for neonatal and infant care. The heated wire connector can overheat, causing smoke or melting, and may lead to airway obstruction or breathing distress in infants. Consumers should stop using the affected circuits and contact Medline Industries for instructions.

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• openFDA · September 2, 2026Moderate risk

  IMRIS Imaging Inc : ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2…

  IMRIS Imaging Inc is recalling its ORT200 operating room table, including reconditioned covered table assemblies with part numbers 113821-600 and 114148-000. The linear actuator and rotational lock can fail, causing unintended table movement that may injure patients during procedures. Consumers should contact IMRIS Imaging Inc for instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY,…

  Medline convenience kits labeled Major Procedure, Operative Lap P&S Surgical, and Laparoscopy (SKUs CDS982040U, DYNJ89608, DYNJ903479L, DYNJ903479M) are affected. The kits contain a potentially contaminated component, exposing patients to infection risk. Consumers should stop using the kits and contact Medline for instructions.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN…

  Medline Industries is recalling four convenience kits, including CMH Litho Minor Pack-LF and GYN Laparotomy, sold nationwide. The kits contain a potentially contaminated component, exposing patients to risk of infection. Consumers should stop using the affected kits and contact Medline for return or replacement.

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• openFDA · September 2, 2026Moderate risk

  Medline Industries, LP : Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY,…

  Medline Industries is recalling four convenience kits labeled LAMI FUSION, NON MB MJR NEURO CRANI SM PK, CRANIOTOMY, and KIT CRANIOTOMY RFD with specific SKUs. The kits contain a potentially contaminated component, exposing patients who use them to risk. Consumers should stop using the recalled kits and follow Medline's recall instructions.

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• openFDA · September 2, 2026Moderate risk

  Apotex Corp. : Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured…

  The recall affects Paxil CR (paroxetine) extended-release tablets, 37.5mg, 30-count bottles, made by Apotex Corp. The tablets failed dissolution and 24-month stability tests, so they may not dissolve properly, and patients nationwide are exposed. Consumers should stop using the recalled tablets and contact their pharmacist or doctor for guidance.

  drugs
• openFDA · September 2, 2026Moderate risk

  ACCORD HEALTHCARE, INC. : Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured…

  Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 112 mcg, 1000-count bottles. The tablets may be subpotent, posing a health risk to patients who take this thyroid medication. Consumers should check their bottles and follow the recall instructions.

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• openFDA · September 2, 2026Moderate risk

  ACCORD HEALTHCARE, INC. : Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured…

  Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 88 mcg, 1000-count bottles. The tablets are subpotent, meaning they may not work as intended, affecting patients who take this thyroid medication. Consumers should stop using the recalled bottles and return them to their pharmacy or consult their healthcare provider.

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• openFDA · September 2, 2026Moderate risk

  ACCORD HEALTHCARE, INC. : Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), packaged in a) 90-count bottles (NDC 16729-451-15) and b) 1000-count bottles, (NDC 16729-451-17), Rx Only,…

  Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg) in 90-count and 1000-count bottles. The tablets are subpotent, meaning they may contain less active ingredient than labeled, affecting patients who take this thyroid medication. Consumers should follow the recall instructions provided by the FDA or their pharmacy.

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• openFDA · September 2, 2026High risk

  B BRAUN MEDICAL INC : Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00

  B. Braun Medical Inc. is recalling Lactated Ringer's Injection USP, 1000 mL EXCEL containers. The IV solution may contain particulate matter, posing a risk of injury to patients who receive it. Consumers should stop using the recalled product and return it to their pharmacy or contact B. Braun Medical for instructions.

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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.