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.
Boston Scientific recalls CRE Pro Wireguided 15-18mm 240cm devices with potential sterile pouch breaches. Affected units have specific lot numbers and expiration dates. Consumers should contact the company for details.
Bard recalls specific PowerPICC SV catheter models due to lidocaine ampoules being manufactured under deficient practices. Affected units have unique UDI-DI codes and lot numbers. Consumers should check their catheters for these identifiers.
Elekta recalls MOSAIQ Oncology Information System software version 3.2 due to potential failure to load adapted baseline shift plans during treatment, risking incorrect radiation therapy delivery.
Boston Scientific recalls CRE Pro Wireguided 10-12mm 240cm catheters due to potential sterile breach in packaging. Affected units have specific lot numbers and expiration dates. Consumers should check their packaging for the lot numbers listed.
Medline recalls 10 types of convenience kits containing Huons Lidocaine Ampules due to FDA-identified quality issues from manufacturing inspections.
