Recall database

Ongoing recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1,093–1,104 of 4,550 recalls

Class IOngoingZ-1568-2026

Erbe USA Inc recalls Flexible Cryoprobe (OD 2.4mm

Probes may rupture/burst during activation

Erbe USA IncGAApr 1, 2026

Class IOngoingZ-1567-2026

Erbe USA Inc recalls Flexible Cryoprobe (OD 1.7mm

Probes may rupture/burst during activation

Erbe USA IncGAApr 1, 2026

Class IOngoingZ-1566-2026

Erbe USA Inc recalls Flexible Cryoprobe (OD 1.1mm

Probes may rupture/burst during activation

Erbe USA IncGAApr 1, 2026

Class IIIOngoingZ-1587-2026

Datascope Corp. recalls Battery Charging Station

The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP.…

Datascope Corp.NJMar 25, 2026

Class IIOngoingZ-1586-2026

Hologic, Inc. recalls Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303…

Due to product exhibiting potential to generate either invalid or false negative results.

Hologic, Inc.CAMar 25, 2026

Class IIOngoingZ-1585-2026

Diagnostica Stago, Inc. recalls Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF…

After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.