Recall database

Class II recalls

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

Showing 505–516 of 3,866 recalls

Class IIOngoingZ-2077-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2076-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2075-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2074-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2073-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2072-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2071-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2070-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2069-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLCMOMay 13, 2026

Class IIOngoingZ-2068-2026

Mint Medical GmbH recalls Mint Lesion

If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.

Mint Medical GmbHMay 13, 2026

Class IIOngoingZ-2067-2026

BioFire Diagnostics, LLC recalls BioFire Joint Infection (JI) Panel REF: RFIT-ASY-0138

Contamination to in-vitro diagnostic test may result in false positives.

BioFire Diagnostics, L…UTMay 13, 2026

Class IIOngoingZ-2065-2026

Physio-Control, Inc. recalls LIFEPAK 15

Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intende…

Physio-Control, Inc.WAMay 13, 2026