Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
FDA recalls eTRAX Needle System Starter Kit 18G due to an error in sensor inspection and programming. The needle tip position may be incorrectly identified on the user interface.
Burlington Medical is recalling Wrap Aprons due to potential degradation of Xenolite 800 attenuation material over time. Approximately 5,198 units distributed worldwide are affected.
Infusion sets may contain dull or blunt needle tips that could be difficult to advance or break during insertion, creating potential complications.
Mentor's CPX 4 breast tissue expanders may contain dull or blunt needle tips that could break or resist advancement during saline injection, potentially hindering treatment.
Medtronic's Paradigm REAL-Time Veo insulin pumps (55,724 units) may deliver incorrect insulin amounts when elevated or lowered relative to the infusion site, risking severe low or high blood sugar episodes.
Burlington Medical, LLC is recalling leg wraps with Xenolite 800 material that may degrade over time and lose effectiveness. The recall affects 103 units distributed worldwide.
Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments due to broken or frayed grip cables. The defect could impair surgeon control during surgical procedures.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently on the Allura Xper FD20/15 OR Table when using the wired foot switch. This malfunction could impact imaging-guided surgical procedures.
Civco Medical Instruments is recalling eTRAX Needle Sensor - 18G units due to an inspection and programming error that may cause incorrect needle tip position identification on the user interface.
The MiniMed 620G insulin pump may deliver incorrect insulin amounts when the pump is raised or lowered relative to where it's inserted, risking severe low or high blood sugar and serious complications.
Philips Azurion 3 M12 X-ray systems are recalled due to wired foot switch malfunction that may prevent or interrupt X-ray imaging initiation. A total of 298 units are affected.
Philips recalled Azurion 7 B20 X-ray systems due to foot switch malfunction that may prevent imaging initiation. Affects 1,523 units worldwide.
Burlington Medical recalled 14,323 frontal aprons due to potential degradation of Xenolite 800 attenuation material. The material may lose effectiveness over time, reducing protective capacity.
Medtronic recalls its MiniMed 780G insulin pump due to unintended insulin over- and under-delivery when the pump is elevated or lowered relative to the infusion site. The dosing errors can result in severe hypoglycemia or hyperglycemia.
Medtronic MiniMed 640G insulin pumps can deliver too much or too little insulin when elevated or lowered relative to the infusion site, potentially causing severe low or high blood sugar emergencies.
The RefleXion X1 Radiotherapy System software fails to carry forward angular roll corrections into treatment delivery, potentially displacing radiation dose and causing 10-20% underdose. The recall affects 12 systems across 8 U.S. states.
Mentor Texas is recalling CPX 4 US Breast Tissue Expanders because the infusion needle sets may have dull, blunt, or broken tips that can fail during use.
Burlington Medical Blockers radiation shielding devices are recalled for potential degradation of attenuation material that could reduce shielding effectiveness over time.
Intuitive Surgical is recalling da Vinci S and Si Monopolar Curved Scissors instruments due to increased reports of broken or frayed grip cables. These reusable surgical instruments transmit motion through cables that could malfunction during endoscopic procedures.
Azurion 5 M20 X-ray systems may fail to start imaging due to wired foot switch malfunction. No injuries reported.
Philips has recalled the Allura Xper FD20/20 operating room X-ray table due to wired foot switch defects that may prevent or intermittently delay X-ray imaging. Five affected units have been distributed internationally.
Olympus is recalling SOLTIVE Pro Laser Systems with defective 24V power supply modules that may cause device malfunction, smoke, or burning smell. 32 units distributed worldwide.
Medline convenience kits containing Olympus biopsy valves are being recalled due to rubber fragments detaching from the valve slit. This could create a foreign body in a patient's airway, potentially requiring removal and causing breathing complications.
Medline Industries is recalling 420 units of Sterile Radiology Procedure Kits (Model DYNDH1491B, Lot 25GBB924) due to a potential breach in sterile pouch packaging that may compromise product sterility.
SUMMA THERAPEUTICS recalled the Finesse BTK Multicath balloon catheter due to the potential that the balloon may not meet burst specifications. The recall affects 22 units in New Jersey and Florida.