FDA Recall Terminated

Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna.

Recall: Z-2877-2018 · Initiated April 16, 2018

Recall

Recall Number
Z-2877-2018
Event Number
80487
Firm
TriMed Inc.
FEI Number
3001236812
Product Code
HRS
Status
Terminated
Root Cause
Process control
Initiated
April 16, 2018
Terminated
January 28, 2021
Address
27533 Avenue Hopkins, Santa Clarita, CA, 91355-3910

Description

Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna.

Reason

Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate

Action

Tri-Med issued notification on April 16, 2018 requesting: Determine the lot number of all Ulnar Osteotomy Compression Plates, Short (UOCP-S) .If you have UOCP-S plates with the lot numbers listed (10003, 10017): o Remove the UOCP-S plates from the tray and quarantine it. Do not use this plate. Contact TriMed at [email protected] or call 800-633-7221. TriMed will arrange have the plate(s) returned to the company and replaced. Return the Recall Response card attached to this letter to TriMed as soon as possible. Contact TriMed via telephone or email as per below if you have any questions: Telephone*: 800-633-7221, Email: [email protected]. TriMed will replace the potentially defective plates with plates that have been manufactured and confirmed to meet TriMeds specifications.

Distribution

Worldwide Distribution in the state of TX and countries of Australia, China Sweden

Quantity

722