Biomet, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2058-2015)

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:

A.L.P.S., 3.5mm x 60 mm Cortical Locking Screw. Bone fixation screw

Product Classification:

Class II

Date Initiated: June 4, 2015

Date Posted: July 22, 2015

Recall Number: Z-2058-2015

Event ID: 71423

Reason for Recall:

Sterile packaging was not sealed. The implantation of an unsterile screw may lead to infection.

Status: Terminated

Product Quantity: 50 units

Code Information:

Part number:856135060 Lot: 061300

Distribution Pattern:

Domestic: None. International: Netherlands and Japan

Voluntary or Mandated:

Voluntary: Firm initiated