FDA Recall Terminated

EVOS Screws - Product Usage: is a part of the EVOS MINI plating system, indicated for fracture fixation, arthrodesis, reconstruction, replantation or reduction of small bones and small bone fragments.

Recall: Z-2945-2020 · Initiated August 24, 2020

Recall

Recall Number
Z-2945-2020
Event Number
86342
Firm
Smith & Nephew, Inc.
FEI Number
1020279
Product Code
HRS
Status
Terminated
Root Cause
Error in labeling
Initiated
August 24, 2020
Terminated
July 11, 2022
Address
1450 E Brooks Rd, Memphis, TN, 38116-1804

Description

EVOS Screws - Product Usage: is a part of the EVOS MINI plating system, indicated for fracture fixation, arthrodesis, reconstruction, replantation or reduction of small bones and small bone fragments.

Reason

Multiple or incorrect expiration dates were provided on the affected designation labels.

Action

On August 24th the firm sent via email a notification to affected consignees. Consignees are asked to inspect inventory, locate and quarantine affected devices. Sales Reps and or distributors are instructed to notify customers of the field action and ensure required actions are complete. Affected product will be returned to Smith & Nephew. All consignees are asked to complete a Response Form, even if they do not have product to return.

Distribution

International Distribution to the countries of Denmark, Sweden, France and Spain.

Quantity

71 units