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.
Recalled AART Silicone Carving Implants (models 600-601 to 600-804) due to FDA approval issues. Check UDI-DI codes and lot numbers for affected items.
Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection tubes (model 07 7450) produced from August 2023 to February 2025 due to inadequate quality control. Consumers should contact the company for details.
Anatomy Supply Partners recalls SAFE-T-FILL Magnetic Rings (Model 07 9502) due to inadequate quality control during manufacturing. Affected units were produced from June 2022 to February 2025. No specific action is required as the hazard is not immediately dangerous.
Zimmer Biomet recalls Dual Mobility Vivacit-E bearings with size mixup risk. The package labels a Size F but contains Size G implants, potentially causing improper fit.
