FDA recall Z-1279-2024

Product

D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.

Reason for recall

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

Distribution

US Nationwide distribution in the state of ME.

Key facts

Status

Ongoing

Initiation date

2023-10-06

Report date

2024-03-20

Voluntary/Mandated

Voluntary: Firm initiated

Location

Tuttlingen, N/A, Germany

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1279-2024