Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,021–1,032 of 2,088 recalls
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
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.
Contamination to in-vitro diagnostic test may result in false positives.