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
2026 device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 613–624 of 1,678 recalls
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
Class IIOngoingZ-2064-2026
Erbe Medical, LLC recalls ERBEFLO 2
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip under unsupported thi…
Erbe Medical, LLCAZMay 13, 2026