Biomet, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0381-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Use Only. Designed to release the transverse carpal ligament.

Product Classification:

Class II

Date Initiated: October 25, 2013

Date Posted: December 4, 2013

Recall Number: Z-0381-2014

Event ID: 66792

Reason for Recall:

Security Blades were manufactured oversized and potentially won't advance or may be difficult to advance through the mating Security Clip.

Status: Terminated

Product Quantity: 1130

Code Information:

Catalog Number: 200068 Medical Device Listing Number: B008657 Lot Number Identification: 088610, 090600, 143810, 257060, 289900, 365910, 460490, 558300, 626660, 697320,767260,795090,857730,864640,979680

Distribution Pattern:

Worldwide Distribution: USA (nationwide) and Internationally to Japan.

Voluntary or Mandated:

Voluntary: Firm initiated