Browse through 642 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Boothwyn Pharmacy recalled 8 vials of Fluorescein 2% Ophthalmic Solution on July 9, 2025. The recall occurred due to the drug being subpotent, posing potential health risks. Consumers should stop using the product immediately and seek guidance from their healthcare provider.
Boothwyn Pharmacy recalled 648 vials of Semaglutide injection on July 9, 2025. The product is subpotent and poses a high hazard risk. Consumers should stop using the product immediately and contact their healthcare provider.
Boston Scientific Neuromodulation recalled 25,260 deep brain stimulation systems on July 8, 2025, due to wire break issues. Users may experience loss of therapy and other serious complications. Patients should stop using the devices immediately and seek further instructions.
Rite Aid recalled 984,000 first aid alcohol prep pads on July 7, 2025, due to subpotent isopropyl alcohol levels. The affected product may not effectively disinfect, posing health risks to users.
Medline Industries recalled approximately 6.67 million alcohol prep pads on July 7, 2025. The recall stems from isopropyl alcohol levels falling below the labeled concentration. Consumers should stop using the product immediately and seek guidance from healthcare providers.
H-E-B recalled 300,000 units of inControl Sterile Alcohol Pads on July 7, 2025. The recall follows reports that isopropyl alcohol levels fall below the labeled concentration. Consumers should stop using the product immediately.
CURAD recalled 1,639,996 alcohol prep pads on July 7, 2025. The recall addresses subpotent isopropyl alcohol levels that fall below labeled concentration. Consumers should stop using these products immediately.
Walmart recalled 3.46 million ReliOn Sterile Alcohol Swabs on July 7, 2025. The swabs contain isopropyl alcohol levels below the labeled concentration. Consumers should stop using the product immediately.
Good Neighbor Pharmacy recalled 66,000 alcohol prep pads on July 7, 2025. The product failed to meet isopropyl alcohol concentration standards. Consumers should stop using the product immediately.
Evergreen Orchard Farm recalled 610 cases of Korean Pear Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The affected product was distributed to Pennsylvania, New Jersey, and New York. Consumers should not consume this juice and are advised to seek refunds or replacements.
Evergreen Orchard Farm recalled 78 cases of grape juice on July 3, 2025, due to a lack of pasteurization and sanitation records. The recall affects products distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds.
Tandem Diabetes Care recalled 19 t:slim X2 Insulin Pumps on July 3, 2025, due to an app defect. The defect affects devices when set to right-to-left languages, potentially causing incorrect therapy decisions. This may lead to hypoglycemia or hyperglycemia.
Evergreen Orchard Farm recalled 197 cases of Jujube Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The juice was distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds immediately.
North American Rescue recalled 552 Junctional Emergency Treatment Tools on July 1, 2025. The device may have a manufacturing defect that compromises its structural integrity. Healthcare providers should stop using it immediately and follow recall instructions.
CHETAK NEW YORK recalled 5,232 packets of Deep Sprouted Mat on June 28, 2025. The product tested positive for Salmonella, a serious health risk. Consumers in CA, NJ, IL, FL, and TX should not consume the product and seek refunds.
bioMerieux recalled 235,269 VITEK 2 Gram-negative AST Test Kits on June 26, 2025. The recall follows potential false resistant results for Colistin with specific bacteria. This may affect patient treatment decisions in multiple countries.
BulkSupplements.com recalled 1,001 units of Inositol powder on June 25, 2025, due to potential contamination with Staphylococcus aureus. The recalled products include 250g, 500g, and 1kg packages sold in the U.S. and several international locations.
Orthofix U.S. recalled three intervertebral body fusion devices on June 24, 2025. A labeling error states the width as 33 mm instead of the correct 37 mm. Patients and healthcare providers must stop using the device immediately.
Nirwana Foods recalled its Golden Raisin product on June 23, 2025, due to undeclared sulfites. This recall affects bags sold in New Jersey and New York. Consumers should not consume the product and seek a refund.
Quidel Corporation recalled 22,470 Dipstick Strep A Tests on June 17, 2025, due to potential false positive results. The recall affects tests distributed in multiple U.S. states and internationally. Patients and healthcare providers must stop using the device immediately.