HIGH
CPSC
StopBox USA Recalls AR-15 Chamber Lock Pro for Risk of Serious Injury or Death
StopBox USA
A manufacturing
toddler product Recalls
292 recalls tagged with “toddler product”.
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Index Medical Kits Recalled for Re-Gassing After EO Sterilization Non
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
Lutronic XERF EFFECTOR 60 Electrosurgical Unit Recalled for Manufacturing Defects (2025-2026 Models)
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.
Lutronic
Manufacturing defects
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems LKRA40G Radiology Pack Recalled Over Unvalidated Re-sterilization (HIGH)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Medical Convenience Kits Over EO Re-Gassing Risk (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Rire Recall: 32,433 Medical Convenience Kits Recalled for Re-GassedEO
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DRUG
Zydus Chlorpromazine Hydrochloride 200 mg Recall Expands Nationwide Over CGMP Deviations
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Chlorpromazine Hydrochloride
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 OR Table Recalled for 174 Units Worldwide in 2025
Philips Medical Systems Nederland
Systems may
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Gluta Plus Glutathione 60-Capsule Recall for Milk Allergy Hazard
New Spirit Naturals
undeclared allergen
Health & Personal Care
HIGH
FDA DEVICE
Inpeco Recall: 8 FlexLab FLX Potassium Test System Units Over Unverified HIL Function (2025)
Inpeco
The FlexLab
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Faces High-Risk Recall for Allura Xper FD20/15 BIOS Battery
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Bevacizumab Syringe Recall Affects 109,320 Units Nationwide
Lack of Assurance of Sterility
Fagron Compounding Services
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter Recall 2025
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare CLEARLINK CONTINU-FLO IV Set Recalled for Leaks in 2025 (958,351 Units)
Baxter Healthcare
IV sets
MEDIUM
CPSC
DT Swiss Recalls Carbon Wheels Over Crash Hazard Affecting 2740000 ID Codes and Higher (2025)
DT Swiss
A defect
HIGH
CPSC
Party Favors Lite-Up Torches and Laser Pointers Recalled for Battery Ingestion Risk
Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.
Party Favors Lite-Up Torches and Laser Pointers
The recalled
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Verio MRI Recalled Globally Over Ice Blockage Risk in Venting System
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Cima.X MRI Recall: 9 Units Worldwide (2025)
Siemens Medical Solutions USA
There is