1084 alerts recorded, refreshed every six hours. Filter by source or category.
Pacific Health Sciences LLC recalled Organiccs Absolutely Pure Type-1 Hydrolyzed Collagen Peptides capsules. The product contains undeclared crab shell, which poses a risk to people with shellfish allergies. Consumers should stop using the capsules and return them to the place of purchase.
TOJI CO. is recalling Cloud Cafe branded Collagen Milk, Strawberry Milk Zero, Caffeine Free, sold in 10-piece boxes. The product contains undeclared fish, posing a risk to consumers with a fish allergy. Consumers should not drink the recalled milk and should return or discard it.
Todd's Seeds Sprouting Seed Mix, containing broccoli, radish, and alfalfa seeds, is recalled in 1/4 lb, 1/2 lb, 1 lb, and 5 lb bags. The seeds may be contaminated with E. coli and Salmonella, posing a risk to anyone who eats them. Consumers should not eat the product and should discard it or return it for a refund.
The recall affects Khazana The Treasure Spice Magic Fennel Candy in 5-pound poly plastic bags, sold in New York. The candy contains undeclared Yellow 5, Yellow 6, Red 3, and Blue 1, posing a risk to consumers with sensitivities to these dyes. Consumers should not eat the product and should return it to the place of purchase or discard it.
Todd's Seeds LLC is recalling its Alfalfa & Mung Bundle, with each one-pound bag packaged separately in heat-sealed resealable bags. The alfalfa seed may be contaminated with E. coli and/or Salmonella, posing a risk to consumers who purchased nationwide through Amazon or directly. Consumers should consult the FDA recall notice for further instructions.
Todd's Seeds LLC is recalling its Todd's Seeds Variety Pack of Sprouting Seeds containing broccoli, alfalfa, radish, mung, and clover in 2-ounce bags. The seeds may be contaminated with E. coli and/or Salmonella, posing a risk to consumers who purchased the multi-pack nationwide through Amazon or direct orders. Consumers should not eat the recalled seeds and should discard them or return them to the company.
Salata Salad Kitchen Jalapeño Avocado Dressing is recalled by Salata Dressings, LLC. The dressing may contain Salmonella from diced jalapeños, posing a health risk to consumers in Georgia, North Carolina, and Texas. Consumers should not eat it and should return or discard the product.
Coco G's Snack Foods, Inc. is recalling Coco G's Gourmet Flaming Cheddar Hots Spicy Cheddar Cheese Popcorn in plastic bags. The product may be contaminated with Salmonella, posing a health risk to consumers in Illinois and Wisconsin. Consumers should not eat the popcorn and should return or discard it.
Todd's Seeds Broccoli & Friends Sprouting Seed Mix, containing broccoli, alfalfa, radish, and clover, is recalled in various package sizes. The product may be contaminated with E. coli and Salmonella from recalled alfalfa seed, posing a risk to consumers who purchased it nationwide through Amazon or directly. Consumers should stop using the product and discard it or return it for a refund.
Admiral Beverage Corporation recalls 7up Tropical beverage 12-packs of 12oz cans, labeled as 7Up Tropical Zero Sugar but containing full sugar soda. The product contains undeclared sugar, posing a risk to consumers in Utah who need to avoid sugar. Consumers should check the UPC and return or discard the affected product.
The recall affects Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil by LMSI, LLC, sold in 3.4, 8.5, and 17 fluid ounce glass bottles. The product contains garlic essential oil not approved for culinary use, which poses a hazard to anyone who purchased it. Consumers should not consume the product.
Lior brand Cinnamon Ground Seasoning in 90g transparent plastic containers with UPC 794711005484 is recalled. The product contains elevated levels of lead, posing a health risk to consumers in NY, NJ, PA, TX, FL, and IL. Consumers should not eat it and should return or discard the product.
Todd's Seeds is recalling its Salad Sprouting Mixture (Broccoli, Mustard, Alfalfa, Cabbage) in 1/4, 1/2, and 1 lb bags. The product may contain E. coli and Salmonella from recalled alfalfa seed, posing a risk to anyone who eats it. Consumers should not eat the recalled mixture and should discard it or return it for a refund.
YunHeng is recalling LandTale adult portable bed rails with white frames and black foam grips. Users can become entrapped in the bed rail or between it and the mattress, risking asphyxiation and death. Consumers should stop using the recalled bed rails and contact YunHeng for a refund or replacement.
Walmart is recalling over 4.4 million Expert Grill metal wire bristle grill brushes. Small wire bristles can detach and stick to grills or food, posing an ingestion hazard and risk of serious internal injuries to consumers. Consumers should stop using the recalled brushes and contact Walmart for instructions.
LLK Trading is recalling Mochi Malrang Mystery Dumpling Toys. The water beads inside expand larger than allowed and can cause choking, intestinal obstruction, or death if ingested by a child. Consumers should immediately stop using the recalled toys and keep them away from children.
The recall affects Kobayashi's HotHands-branded rechargeable hand warmers, model H163650, sold in packs of two. The lithium-ion battery and electrical components can overheat and ignite, posing a risk of serious injury from fire and burns to consumers. Consumers should stop using the recalled hand warmers and contact Kobayashi for a refund or replacement.
Golden Resale is recalling ZAREI portable camping showers with a bucket and immersion heater. The immersion heater can ignite when partially or completely out of water, posing a fire hazard that can cause serious injury or death to users. Consumers should stop using the recalled showers immediately and contact Golden Resale for a refund or replacement.
Gobi Heat recalled its rechargeable hand warmers, model UT3053, sold in packs of two. The lithium-ion battery and electrical components can overheat and ignite, posing a fire and burn hazard to consumers. Consumers should stop using the recalled hand warmers immediately.
The recalled product is the GBYMIUY magnetic stick figure toy set, sold in packs of 30 multi-colored human-shaped figures. The toys can release loose high-powered magnets, which if swallowed by children can cause intestinal perforations, twisting, blockage, blood poisoning, and death. Consumers should immediately stop using the recalled toy sets and keep them away from children.
Gazelle USA recalls Urban Arrow cargo electric bikes, including Family, Shorty, Cargo L/XL, and Tender 1000/1500 models. The front bolt in the seat post clamping mechanism can break, causing the seat to become loose and posing a fall hazard to riders. Consumers must take the action described in the recall notice.
Dollar Tree Stores is recalling its electric balloon pumps, model 406198, which are pink with a blue handle and two nozzles. The pumps can overheat, posing a burn hazard to consumers who use them. Consumers should stop using the recalled pumps immediately and return them to Dollar Tree Stores for a refund.
Designs Direct recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, models 7927-OZ and 7927-OZ1. When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn hazards to users. Consumers should check the model number on the sticker under the base to see if their lamp is affected.
Agrish adult portable bed rails, models AG-12011, 12014 and 12016, are recalled. Users can become entrapped or fall, risking asphyxiation, injury, or death. Consumers should stop using them and contact Agrish for a refund or replacement.
ABC Trading is recalling Squishy Dumpling and Crazy Squib Ball squishy toys. The water beads inside can expand and cause ingestion, choking, and intestinal obstruction, posing a risk of death to children. Consumers must stop using the recalled toys and return them to ABC Trading.
Medline Industries is recalling its Convenience Kit MAJOR PACK, catalog number DYNJ81325A. The neurological sponges inside may have elevated endotoxin levels, posing health risks like fever, nausea, or neurovascular problems for patients. Consumers should stop using the kits and contact Medline for instructions on return or replacement.
Medline Industries is recalling certain Convenience Kits, including PEDS SINUS PACK, SINUS PACK-LF, NASAL-LF, ENT PACK, and EENT PACK, with specific catalog numbers. The kits contain neurological sponges with potentially elevated endotoxin levels, which can cause febrile response, hypotension, nausea, or other serious health issues for patients. Consumers should stop using the recalled kits and follow the recall instructions for return or disposal.
Philips SmartPath to dStream for 1.5T, 3.0T, XR and 3.0T, and Ingenia Elition X are affected. A software issue can terminate an examination during image reconstruction if scan parameters are manually adjusted beyond available system memory, affecting patients and operators. Consumers should avoid manually adjusting scan parameters that exceed the system's memory capacity.
Philips is recalling its Achieva 1.5T, Achieva 1.5T Conversion, and Achieva 1.5T Initial systems. A software issue can terminate an examination during image reconstruction if manual scan settings exceed available memory, affecting patients receiving MRI scans. Consumers should contact their healthcare provider or Philips for further instructions.
Medline Industries is recalling certain Medline Convenience Kits, including craniotomy packs with catalog numbers DYNJT8784 and DYNJ0369348Q through DYNJ0369348T. The kits contain neurological sponges with potentially elevated endotoxin levels, which can cause fever, nausea, low blood pressure, or neurovascular problems in patients. Consumers should stop using these kits, check the catalog numbers, and follow the firm's return instructions.
Baxter Healthcare Corporation is recalling its PRO+ 36" MRS SURFACE mattress, model P7924A13. The UDI label has an error that may cause incorrect product selection, possibly leading to use with an incompatible bed frame, affecting patients and caregivers. Consumers should contact Baxter Healthcare Corporation for instructions on returning or correcting the affected mattress.
Baxter Healthcare Corporation is recalling its PRO+ MRS Surface for VersaCare mattress, model P3255A08. The UDI label has an error that could cause incorrect product identification or selection, leading to use with an incompatible bed frame, affecting users worldwide including the US and Canada. Consumers should contact Baxter Healthcare Corporation for instructions on returning or correcting the product.
Baxter Healthcare Corporation is recalling the VOLARA System, model M08594A, a homecare nebulizer. Contamination in test equipment may have affected the nebulizer flow rate accuracy, exposing users in Colorado and Florida to potential incorrect dosing. Consumers should return the affected device to Baxter for testing.
Becton, Dickinson and Company's ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 is affected. Incorrect switching of channels and flag labels can cause wrong oxygen readings, exposing patients to risk. Consumers should stop using the cable and contact Becton, Dickinson and Company for return instructions.
Philips is recalling its Ingenia Ambition S and Ingenia Ambition X MRI systems with model numbers 781359, 782108, 782139, 781356, 782109, and 782138. A software issue can stop an exam during image reconstruction when scan settings are changed, affecting patients undergoing MRI scans. Users should contact Philips to arrange for a software update or correction.
Ventec Life Systems is recalling its HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve. The oxygen cylinders lack required medical gas labeling, posing a risk to patients using the system. Consumers should follow the recall instructions from Ventec Life Systems.
Medline convenience kits containing Healthmark Instrument Channel Brushes, models SINUS PACK DYNJ48258D and DYNJ48258F, are affected. The brush end may have a sharp edge or burr, posing cut injury, abrasion, and infection risks to users. Consumers should stop using these kits and contact Medline for return or replacement.
Philips North America is recalling its Intera 1.5T MRI systems, including models 781195, 781295, 781175, 781172, 781173, 781104, and 781171. A software issue can terminate an examination during image reconstruction if scan parameters exceed available memory, affecting patients undergoing MRI scans. Consumers should contact their healthcare provider or Philips for further instructions.
AVID Medical, Inc. is recalling the Halyard IV START KIT NON-STERILE, model KRIV26-01, containing BD ChloraPrep Clear 1 mL Applicators. The applicator packaging may have an open or incomplete seal, exposing patients nationwide to a loss of sterility. Consumers should stop using the affected kits and contact AVID Medical for instructions.
Medline Industries is recalling several Medline Convenience Kits for neurological procedures, including Major Neuro VCH, Neuro Pack-LF, Craniotomy Pack, and others. The kits contain neurological sponges that may have elevated endotoxin levels, posing risks like febrile response, hypotension, or nausea to patients. Consumers should stop using the recalled kits, verify catalog numbers, and contact Medline for instructions.
CooperSurgical Inc. is recalling its INCA Infant Nasal CPAP Complete Set with Stay-Flex tubing, model numbers 44-2707, 44-2709, 44-2710, 44-2712, and 44-2715. The tubing may have a loose connection to the nasal cannula, causing loss of CPAP pressure and decreased oxygenation in infants. Consumers should stop using the affected sets and contact CooperSurgical for replacement.
The recalled product is the SeaSpine Mariner Deformity Extended Polyaxial Head, Attached Gimbal, 12mm REF MD1-300010-12. The proximal thread depth is out of design specification, posing a hazard to patients who receive this spinal device. Consumers should contact SeaSpine Orthopedics Corporation for further instructions.
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234 is affected. A software issue displays the doppler sample shallower than its actual location, causing inaccurate blood flow velocity measurements and misdiagnosis for patients. Consumers should follow the voluntary recall instructions from the firm.
Midmark IQvitals Zone, model 1-200-0360 with kit 4-000-0724, is affected. The device may give inaccurate blood pressure readings when using the Linear Deflation Method, affecting adult and pediatric patients. Consumers should contact Midmark Corporation for further instructions.
Olympus is recalling the BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector, model CD-B612LA. The ceramic tip may detach during surgery because the device was made without enough adhesive, posing a risk to patients. Users should stop using the affected probes and contact Olympus or their healthcare provider for return and replacement instructions.
Philips North America is recalling its Ingenia 3.0T and Ingenia 3.0T CX MRI systems, including model numbers 781342, 781377, 782103, 781271, and 782105. A software issue can terminate an examination during image reconstruction if scan parameters are manually adjusted to exceed system memory, affecting patients undergoing MRI scans. Consumers should follow the recall instructions from Philips and the FDA.
Cardinal Health 200, LLC is recalling certain Presource Convenience Kits with catalog numbers PVMHIVMHD, PVMHIVM14, and PVMHIVM15. The kits contain applicators that may have an open or incomplete seal, exposing users to possible skin, soft tissue, or systemic infection. Consumers should check their kits for these catalog numbers and follow the firm's voluntary recall instructions.
Maquet SAS is recalling its PowerLED 300 Concealed Lighting System, models ARD568474114A and ARD567501286. The device can detach at the junction between the spring arm and suspension arm and fall, posing injury risk to users. Consumers should follow the recall instructions from Maquet SAS, as this is a voluntary firm-initiated recall.
Philips North America is recalling its Evolution upgrade 1.5T and 3.0T MRI systems, model numbers 782116, 782148, 782117, and 782143. A software issue can stop an exam during image reconstruction when manual scan parameter changes exceed available memory, affecting patients undergoing MRI scans. Consumers should contact their healthcare provider or Philips for further instructions.
Ventec Life Systems is recalling its HomeFill Oxygen System and HomeFill Cylinder M9 with Integrated Conserver. The oxygen cylinders lack required medical gas labeling, which can confuse users and pose a risk to patients. Consumers should stop using the affected devices and contact Ventec Life Systems for instructions.
Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.