Recalls and Product Safety Alerts
Our Product Safety Team proactively investigates and addresses reported safety complaints and incidents to ensure customer protection from potential product-related safety risks. We closely monitor public recall alert websites and receive notifications from vendors and sellers. Upon discovering a product recall, we immediately halt affected product offerings, and promptly inform both customers and sellers involved about the recall. For more information visit our Safety Information, Recalls and Legal Notices Page .
Search for recalls and alerts
Please, note that this list includes public alerts starting from 2024. This list may not be exhaustive and it only includes alerts for products sold on Amazon.
September 4, 2027
SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine
September 1, 2027
Class 2 Device Recall Medline
September 27, 2026
Public Recall : Philips recall Ingenia Blue Seal SE due to When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.
September 27, 2026
Public Recall : Merit recall Embosphere Microspheres due to Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, which if used could lead to infection.
September 27, 2026
Class 2 Device Recall MR 7700
September 27, 2026
Sempio Food Services Inc. Recalls Ready-To-Eat Chicken Stew Products Imported Without the Benefit of Import Reinspection
September 27, 2026
Class 2 Device Recall hCG Pregnancy Test Strips (Urine)
September 27, 2026
Class 2 Device Recall hCG Pregnancy Test Device (Urine/Serum), hCG Pregnancy Test Device (Urine)
September 27, 2026
Class 2 Device Recall hCG Pregnancy Test Device (Urine)
September 27, 2026
Class 2 Device Recall ACS, American Contract System
September 27, 2026
Public Recall : American Contract Systems - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays due to Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).
September 27, 2026
Public Recall : Philips recall Philips IntraSight Plus due to Software may associate image data from one patient with another patient's record, The software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.
September 27, 2026
Public Recall : Performance Pro Blue Nitrile Patient examination gloves due to Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.
September 27, 2026
Class 2 Device Recall Opportunity Flex
September 27, 2026
Class 2 Device Recall Opportunity Pro
September 27, 2026
Ford Motor Company (Ford) is recalling certain 2026 Ranger vehicles equipped with a 10.1-inch center stack screen. The screen may lose power and fail to display the rearview camera image. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."
September 27, 2026
Class 2 Device Recall MR 5000 Series
September 27, 2026
Class 2 Device Recall Ingenia
September 27, 2026
Fontanini Foods LLC Recalls Raw, Frozen Pork Sausage Products Due to Possible Foreign Matter Contamination
September 27, 2026
Public Recall HeartSine SAM 350P, HeartSine SAM 360P and HeartSine SAM 450P due to Electrical/Mechanical, Two issues identified: (1) Membrane tail defect in internal component causing intermittent fault that can occur while device is holding charge, delivering shock, or after shock delivery, rendering device inoperable; (2) Limited number of devices distributed without required maintenance supplement containing periodic maintenance instructions as risk control measure
Further information on alerts can be accessed by clicking the links.
