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.
Paragon 28 recalls P28 Phantom Hindfoot Nail System due to potential sterile packaging breaches. Affected units have specific model and lot numbers. Consumers should check their product details and contact the company for guidance.
Medtronic Neurosurgery recalls Ventriculostomy Kit REF 461: endotoxin levels may exceed safe limits for cerebrospinal fluid contact, causing inflammation. Affected units sold with UDI-DI 00673978947396 and Lot 2025-08779.
Sun Pharmaceutical recalls Perampanel CIII 6mg tablets due to label mix-up with 10mg tablets. Affected units contain incorrect labeling that may lead to incorrect dosing.
BD recalls 60-inch non-DEHP minibore extension sets with UDI-DI codes 10885403236235, 10885403274619, and 10885403237218 due to potential inadequate sterilization processing.
WASPLab W087 devices with WebApp versions 2.33.1, 2.33.3, and 2.34.2 may prevent overwriting results. Consumers should check their software version and contact support for updates.
