Vehicles & Parts
HIGH
NHTSA
BMW Recalls 2025-2026 X1/X2 and MINI Vehicles for Front Seat Belt Retractors (High Risk)
BMW
A damaged
explosion risk Recalls
77 recalls tagged with “explosion risk”.
HIGH
CPSC
HTRC and Haisito T400 Battery Chargers Recalled for Fire Hazard (2026)
Huizhou Haitan Technology Co., Ltd., of China
The chargers
HIGH
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Vancomycin HCI Recall: 34,260 Bags with Break-Off-Part Risk (2026)
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron Compounding Services
Lack of
Health & Personal Care
HIGH
FDA DRUG
Teva Clonidine Transdermal System Recall Expands Over CGMP Deviations, 124,054 Cartons Affected (202
CGMP Deviations: use of an unapproved raw material
CLONIDINE TRANSDERMAL SYSTEM
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled Over Expired-Lot
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Arterial Pressure Monitoring Tray Recalled Over Expired Shelf-Life Labeling (Z-1778-202
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set for Expired-
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical CTO-6 Micro Wire Guide Recalled Worldwide Over Expired Shelf Life Labels (2026)
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Multipurpose Drainage Catheter Recalled Over Expired Labeling in Lots G29775
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Approach CTO-12 Micro Wire Guide Recall Affects 49 Units for Expired Shelf-Life Labels
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Wayne Pneumothorax Tray Recalled for Expired-Labeled Shelf Life (2026)
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Spectrum Central Venous Catheter Tray Recalled for Expired Shelf Life Labels (2026)
Cook Medical recalled 1,872 units of Spectrum Central Venous Catheter Trays worldwide due to expiration dates labeling that exceed true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions."
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Recall: Cook Staged Extubation Set Labeled with Expired Dates in 2026 Class II Recall
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Recall: Strange Bile Duct Stone Exploration Set Labeled with Expired Dates (Z-1784-2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical CTO-18 Micro Wire Guide Recall Affects 75 Units Over Expired Dating (2026)
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.
Cook
Products from
Vehicles & Parts
HIGH
NHTSA
Toyota recalls 2022-2025 Tundra and Tundra Hybrid over reverse light moisture risk
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2022-2025 Toyota Tundra and Tundra Hybrid vehicles. Moisture may enter the reverse light assemblies and cause a light failure.
Toyota Motor Engineering & Manufacturing
Reverse light
Health & Personal Care
HIGH
FDA DEVICE
Philips ALLURA Xper FD20 Recall for 5,084 Units Over Intermittent X-ray Imaging (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10C X-ray System Recall for 15 Units Worldwide (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Tag Statistics
Total Recalls
77