FDA Recall Terminated

LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, and non-unions of the radius and other small bones.

Recall: Z-1949-2016 · Initiated May 2, 2016

Recall

Recall Number
Z-1949-2016
Event Number
74082
Firm
Synthes (USA) Products LLC
FEI Number
3008812560
Product Code
HRS
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
May 2, 2016
Posted
June 10, 2016
Terminated
December 9, 2016
Address
1301 Goshen Pkwy, West Chester, PA, 19380-5986

Description

LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, and non-unions of the radius and other small bones.

Reason

Product incorrectly packaged. The labels on the outside of the box and on the LCP Dia-Meta Volar Distal Radius Plate inside the box are correct; however, the preprinted box which contains the LCP-Dia-Meta Volar Distal Radius Plate is incorrect. The box is preprinted for a 4.5 mm LCP Condylar Plate - Distal Femur.

Action

DePuy Synthes sent out an Urgent Notice to customers informing them of a package mixup and the impact it could have on users. Customers were asked to evaluate their inventory and immediately remove the affected lot (9890811) from stock. Customers were asked to call DePuy Synthes at 1800-479-6329 to obtain a Return Authorization Number for return of the affected product, fill out the verification section of the letter and mail with the product to: Credit/Returns, DePuy Synthes, 1101 Synthes Avenue, Monument, CO 80132. Any questions, they were said to call 610-719-5450 or to contact their DePuy Synthes Sales Consultant.

Distribution

Distributed to one customer: Colorado

Quantity

6 units