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 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
Class 2 Device Recall Presource Packs
September 27, 2026
Public Recall : American Contract Systems recalls CARDIAC HEART BUNDLE NS - OPEN HEART 2 RCH 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 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
September 27, 2026
Class 2 Device Recall hCG Pregnancy Test Device (Urine/Serum)
September 26, 2026
Class 2 Device Recall NOxBOXi Nitric Oxide Delivery System
September 26, 2026
Class 2 Device Recall MR 7700
September 26, 2026
Class 2 Device Recall PALACOS RG pro 40; PALACOS RG pro 80
September 26, 2026
[Shanghai United Imaging Healthcare Co., Ltd.] [Positron Emission Tomography and Computed Tomography System, Model: uMI Panorama GS with software]
September 26, 2026
Class 2 Device Recall PALACOS MV pro 40; PALACOS MV pro 80
September 26, 2026
Class 2 Device Recall Presource Packs
September 26, 2026
G. L. Mezzetta Inc. Announces Recall of Mezzetta Brand Golden Greek Peperoncini (Medium Heat) Due to Presence of Pest Contaminant in the Jar
September 26, 2026
Class 2 Device Recall Presource Packs
September 26, 2026
Class 2 Device Recall Ingenia
September 26, 2026
Class 2 Device Recall uCT 780
Further information on alerts can be accessed by clicking the links.
