FDA Recall Terminated

Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of plates and is intended to provide internal unicortical or bicortical bone fixation.

Recall: Z-1510-2020 · Initiated October 1, 2019

Recall

Recall Number
Z-1510-2020
Event Number
84030
Firm
Arthrex, Inc.
FEI Number
1220246
Product Code
HWC
Status
Terminated
Root Cause
Employee error
Initiated
October 1, 2019
Terminated
September 8, 2021
Address
1370 Creekside Blvd, Naples, FL, 34108-1945

Description

Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of plates and is intended to provide internal unicortical or bicortical bone fixation.

Reason

Screws provided in the device package are 6 mm longer than intended.

Action

Arthrex notified customers of the recall on about 10/01/2019, via "URGENT: REMOVAL NOTIFICATION" letter. Customers were informed that the Low Profile Screw, labeled as 4.5 x 20 mm, in their package measures 6 mm longer than intended. Customers were instructed to immediately discontinue use, sale, and distribution of affected screws and to acknowledge receipt of the recall notification. Direct customers were directed to contact Anthrex Product Surveillance at 866-267-9138 or [email protected]. Arthrex agencies were directed to contact Arthrex Field Logistics Services at [email protected] as soon as possible to arrange for return of affected products. An email also accompanied the recall letter and requested that customers return all affected product. Questions can be addressed to Arthrex Product Surveillance at 866-267-9138 or [email protected].

Distribution

US distribution to MA, MN, ND, OH, SD, TN. International distribution to Australia, Korea, China

Quantity

20 units