Biomet, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1741-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Unilateral external fixation ankle clamp Product Usage: Unilateral external fixation for use treatment of bone conditions amenable to treatment by use of external fixation modality

Product Classification:

Class II

Date Initiated: May 1, 2015

Date Posted: June 17, 2015

Recall Number: Z-1741-2015

Event ID: 71255

Reason for Recall:

Ankle clamp was assembled incorrectly; the offset of the pin to the pivot point is reversed. This prevents complete range of motion and if pushed too far may loosen the pin from the bone. A revision surgery may be necessary to adequately reconnect the fixator to the bone.

Status: Terminated

Product Quantity: 19

Code Information:

Part 14-450510 Lots:268000, 466170, and 813950

Distribution Pattern:

US Nationwide Distribution in the states of CA, TX, FL, NC, MI, GA.

Voluntary or Mandated:

Voluntary: Firm initiated