Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects a potential defect in the catheter connector lid. Patients and healthcare providers must stop using the device immediately.
B Braun Medical recalled 2,840 anesthesia trays on September 18, 2025. The recall stems from a potential defect in the catheter connector lid position. The product poses a high hazard risk to patients and healthcare providers.
B Braun Medical recalled 48,110 epidural anesthesia trays on September 18, 2025. The recall stems from a potential issue with the catheter connector lid. Healthcare providers and patients must stop using the device immediately.
B Braun Medical recalled 60 units of its Combined Spinal and Epidural Anesthesia Tray on September 18, 2025. The recall stems from the potential for the lid of the catheter connector to be incorrectly positioned. Healthcare providers must stop using the device immediately and follow manufacturer instructions.
B Braun Medical recalled 10,130 units of its Combined Spinal and Epidural Anesthesia Tray on September 18, 2025. The recall affects devices due to a potential misalignment with the catheter connector lid. Healthcare providers and patients must stop using the product immediately.
B Braun Medical recalled 5,770 PERIFIX FX Epidural Anesthesia Trays on September 18, 2025. The recall stems from a potential issue with the lid of the catheter connector. This defect may cause improper operation during procedures, posing serious health risks.
B Braun Medical recalled 2,450 pain management trays on September 18, 2025. The recall stems from a potential issue with the catheter connector lid positioning. This defect poses a high risk to patient safety.
B BRAUN MEDICAL recalled 21,270 epidural anesthesia trays on September 18, 2025. The recall follows concerns about a potential misalignment of the catheter connector lid. Patients and healthcare providers must stop using the device immediately.
Taproom Gourmet recalled 3,547 cases of its 15lb bulk "Broadway" Mix on September 18, 2025. The product lacks an ingredient label and contains undeclared allergens including peanuts, sesame, wheat, and soy. Consumers should not consume the product and seek refunds.
Taproom Gourmet recalled 3,547 cases of its 15lb bulk "Madison" Mix on September 18, 2025. The product lacks a proper ingredient label and contains undeclared allergens including peanuts, almonds, wheat, and soy. Consumers should stop using the product immediately and seek a refund.
Taproom Gourmet recalled 3,547 cases of its "Fifth Avenue" Mix on September 18, 2025. The product lacks an ingredient label and contains undeclared allergens including peanuts, almonds, cashew, and soy. Consumers in NY, NJ, CT, CA, IL, and FL are urged to avoid consumption.
Taproom Gourmet recalled 3,547 cases of its 18lb bulk "Empire" Mix on September 18, 2025. The mix lacks an ingredient label and contains undeclared allergens including cashews and almonds. Consumers should not consume the product and seek a refund or replacement.
Kirkland Signature recalled 3,314.7 lbs of Ahi Tuna Wasabi Poke due to potential Listeria contamination. The recall was initiated on September 18, 2025. Consumers should not consume the product and seek refunds immediately.
Garden Fresh Foods Inc. recalled 540 pounds of sliced green onions on September 18, 2025. The product may be contaminated with Listeria monocytogenes. This recall affects only Washington state.
GE Medical Systems recalled 37 LOGIQ P9 ultrasound systems on September 18, 2025. The devices may display inaccurate liver steatosis data, risking inappropriate clinical decisions. Healthcare providers must stop using the devices immediately and follow recall instructions.
Fisher & Paykel Healthcare recalled 51,144 humidifier devices on September 18, 2025. The humidifiers may fail to alert users when disconnected from power, risking oxygen desaturation and hypoxia. Patients and healthcare providers should stop using the device immediately and follow recall instructions.
Goyal Group recalled 293 sets of aluminium cookware on September 18, 2025. The products contain elevated levels of lead, posing a health risk. Consumers should stop using these items immediately and contact the company for a refund.
GE Medical Systems recalled 31 LOGIQ P10 R4.5 HD ultrasound systems on September 18, 2025. The devices may display inaccurate liver steatosis data, risking inappropriate clinical decisions. Healthcare providers must stop using these devices immediately.
GE Medical Systems recalled 65 units of its LOGIQ P10 series ultrasound device on September 18, 2025. The device may show inaccurate liver steatosis measurements, risking inappropriate clinical decisions. Healthcare providers must cease use immediately and follow recall instructions.
HeartSine Technologies recalled over 1.2 million defibrillator pads on September 18, 2025. The recall affects several models due to defective pins that may disrupt electrical contact. Consumers and healthcare providers should stop using these pads immediately.