Browse through 1,551 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.
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.
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.
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.
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.
Cardinal Health recalled all lots of Salem Sump stomach tubes on September 18, 2025. The recall affects tubes with product codes 264929, 264945, and others due to complaints of valve breakage. Patients and healthcare providers should stop using the devices immediately.
Cook Medical recalled 695 Zenith Alpha 2 Thoracic Endovascular Grafts on September 18, 2025. The recall follows reports that PTFE coating scrapings could cause intravascular embolization during deployment. Patients and healthcare providers must stop using the device immediately.
Cardinal Health 200 recalled Salem Sump PVC gastroduodenal tubes on September 18, 2025. The recall affects all lots sold worldwide due to complaints of Anti-Reflux Valve breakage. Patients and healthcare providers must stop using the devices immediately.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects an unspecified number of units due to a potential connector misalignment. This issue poses a high risk to patient safety and requires immediate action from healthcare providers.
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.
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.
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.
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.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The manufacturer identified a potential issue with the catheter connector lid position. No injuries have been reported, but users should stop using the product 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.
Cardinal Health recalled Salem Sump stomach tubes on September 18, 2025, due to reports of valve breakage. The recall affects all lots of multiple models sold worldwide. Users must stop using these devices immediately to prevent potential harm.
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.
Cardinal Health 200 recalled its Salem Sump PVC tubes on September 18, 2025, due to reports of Anti-Reflux Valve (ARV) breakage. Excessive force during use caused the failures, posing a high hazard to patients. The recall affects all lots distributed worldwide.
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.