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.
SunMed Holdings recalls Broselow Domestic Complete ALS Organizer software (model 7730ALS) due to potential dosing errors for Vecuronium, Flumazenil, and Ketamine. Affected units sold with specific lot numbers.
ICU Medical recalls Plum Duo IV pumps with specific list numbers and software versions due to potential piggyback flush errors that may prevent proper flushing of IV lines.
Philips recalls Allura Xper FD20/10 systems with model 722029 where drip tray wasn't properly installed, risking electrical shorts and system shutdowns.
Diagnostica Stago recalls Asserachrom HPIA kit model 00615 with lot 271288 due to potential false negative results in heparin-induced thrombocytopenia testing. Affected kits may not detect anti-heparin-platelet factor 4 antibodies correctly.
Philips recalls Allura Xper FD20 systems with model 722012 where the drip tray may not be installed, risking coolant contact with electrical parts and system shutdown.
