Synthes (USA) Products LLC: Medical Device Recall in 2020 - (Recall #: Z-2816-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Holes / 93mm - Product Usage: intended for fixation of fractures, osteotomies and non-unions of clavicle, scapula, olecranon, humerus, radius, ulna, pelvis, distal tibia and fibula, particularly in osteopenic bone. Part Number 241.381

Product Classification:

Class II

Date Initiated: July 21, 2020

Date Posted: August 26, 2020

Recall Number: Z-2816-2020

Event ID: 86104

Reason for Recall:

May have one or more dimensional features out of tolerance includes: thread pitch diameter depth, thread minor diameter depth, plate thickness and end length out of tolerance that can potentially result in a reduced locking strength of an LCP screw

Status: Terminated

Product Quantity: 191 units

Code Information:

Lot Number: 29P6036 UDI: 10886982166913

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated