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.
Straumann recalls Emdogain (article numbers 440.230V10 and 475.132V10) due to risk of being used on patients instead of for demonstration purposes only.
Mozarc Medical recalls 12 Fr/Ch catheter tray extensions due to potential packaging seal issues. Affected units have specific lot numbers and UDI-DI codes. Consumers should check their product details to determine if recalled.
Recall of BD Alaris infusion pump modules 8100 and related parts due to risk of under/over-infusion if dropped or jarred. Affected units sold after June 19, 2004.
Mozarc Medical recalls Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components (12 Fr/Ch) due to potential packaging seal issues. Affected units have specific lot numbers and reference codes. No immediate action is required as the hazard is not in active use.
TECHNO-PATH recalls Multichem ID-B (SR103B) positive control serum due to potential false negative HIV test results when used with Alinity i platform. Affected units may cause inaccurate HIV testing.
