Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
VANTIVE US Healthcare recalled 230,596 units of the PRIMSAFLEX M100 Set on January 6, 2026. The recall follows a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.
VANTIVE US Healthcare recalled 93,576 Prismaflex HF1000 Sets on January 6, 2026. The recall addresses a potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately and follow provided instructions.
Karison Foods & Snacks, Inc. recalled 2,760 units of NO SUGAR ADDED BESAN LADDOO on January 6, 2026. The product contains undeclared milk, posing a serious risk to those with dairy allergies. Consumers should stop using the product immediately and seek a refund.
Carrot Top Kitchens recalled 12 units of Lemon & Garlic Hummus on January 6, 2026. The product contains undeclared sesame, posing a serious allergy risk. Consumers should stop use and seek a refund or replacement immediately.
Karison Foods & Snacks Inc. recalled 2,760 units of Alsi Pinni on January 6, 2026. The product contains undeclared milk, posing a serious risk to those with milk allergies. Consumers should not consume the product and seek refunds immediately.
Karison Foods & Snacks recalled 2,760 units of Besan Laddoo on January 6, 2026. The product contains undeclared milk, posing a serious risk to consumers with dairy allergies. The recall affects distribution in New York, New Jersey, and Virginia.
VANTIVE US HEALTHCARE recalled 2,724 OXIRIS SET dialyzers on January 6, 2026. The recall follows reports of potential dislodgement of the deaeration chamber from the Prismaflex Control Unit. Patients and healthcare providers must stop using the device immediately.
VANTIVE US Healthcare recalled 137,576 Prismaflex M150 Sets on January 6, 2026. The recall addresses a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Karison Foods & Snacks Inc. recalled 3,120 units of Punjabi Pinni on January 6, 2026, due to undeclared milk. Consumers with milk allergies risk serious health issues. The product was distributed in New York, New Jersey, and Virginia.
Encore Medical, LP recalled 49 units of the EMPOWR Acetabular System on January 5, 2026. Packaging errors may cause surgical delays, potentially affecting patient safety. Healthcare providers should stop using these devices immediately.
Medline Industries recalled 104,608 units of sterile saline wound wash on January 5, 2026. The product may not have met the required sterility assurance level. Consumers should stop using this product immediately and follow recall instructions.
Medline Industries recalled 8,773 units of its Nail Kit, Model Number DYKM1528, on January 5, 2026. The recall stems from a failure to meet required sterility assurance levels in the saline wound wash. Patients and healthcare providers should stop using the product immediately.
Medline Industries has recalled 3,578,805 units of its sterile saline wound wash due to potential sterility assurance issues. The recall, effective January 5, 2026, affects products distributed worldwide, including in the U.S. Consumers should stop using the product immediately.
Raz Design Inc recalled 66 Raz Mobile Shower Commode Chairs nationwide, citing a modification that may allow the seat to detach if outside rear brackets are not properly engaged. The recall covers multiple catalog numbers and serial ranges. Patients and healthcare providers should stop using the device immediately and contact Raz Design for instructions.
Medline Industries recalled 1,640 units of its Nail Kit, Model POD14214, on January 5, 2026. The recall stems from concerns that the sterile saline wound wash may not meet required sterility standards. Patients and healthcare providers must stop using the product immediately.
Medline Industries recalled 10,550 wound care kits on January 5, 2026, due to potential sterility issues. The recall affects several model numbers, including DYKM1361A and DYKM2013. Consumers should stop using the kits immediately and follow the manufacturer's instructions.
Encore Medical, LP recalled 19 units of the EMPOWR 3D Knee Tibial Insert on January 5, 2026. The recall follows the discovery of a packaging error that may cause surgical delays. Healthcare providers and patients should stop using the device immediately.
Biomerieux recalled 2,668,954 VITEK 2 Gram-negative susceptibility cards on January 5, 2026. The recall addresses potential false resistant results for certain antibiotic tests. Healthcare providers and patients must stop using the product immediately.
Alphatec Spine recalled 7 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The incorrect navigated array connection geometry poses a high hazard risk in surgical settings. Healthcare providers and patients must stop using the devices immediately.
Alphatec Spine recalled 15 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The navigated array connection geometry is incorrect, posing risks during surgical procedures. Healthcare providers and patients should stop using the instruments immediately.