We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.
Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Nipro Medical recalls Hemodialysis System Surdial DX REF: MC+SDX01 (Rx Only) due to screw loosening or falling out. Affected units have serial numbers listed in the recall. Stop using immediately.
Medline recalls specific perfusion syringes due to potential sensitization risks from BD Luer Tip Caps failing biocompatibility tests. Affected units include lot 25FMJ081 with UDI/DI numbers 101934896215321533.
Medline recalls Curad Quick Strip Fabric Bandages due to potential open seals in packaging that could compromise sterility. Affected lots include all units sold. Consumers should check product labels for item numbers.
Medline recalls Curad Germ-Shield Touch-Free Fabric Bandages due to potential open packaging seals that could compromise sterility. Affected lots sold from 2020 onward; check product labels for UDI/DI numbers.
Philips recalls Azurion R3.0 interventional fluoroscopy systems (model 722234) shipped between July 2024 and June 2025 due to missing SSD spacer, which could fail FDA safety requirements for source-skin distance.