FDA Recall Terminated

SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery

Recall: Z-0270-2020 · Initiated October 2, 2019

Recall

Recall Number
Z-0270-2020
Event Number
84017
Firm
Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada
FEI Number
3000327445
Product Code
LXH
Status
Terminated
Root Cause
Device Design
Initiated
October 2, 2019
Terminated
October 26, 2020

Description

SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery

Reason

There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.

Action

Pega Medical notified customers of the recall on about 10/02/2019, via "Urgent Field Safety Notice - Recall" letter. Customers were informed that SCFE Drivers, 6.5mm and 7.3 mm of the Free Gliding SCFE Screw System had issues with the knobs. Specifically the knobs have the potential to have loosened screws, or screws that have fallen out, as a result of the ultrasonic cleaning of the knobs. Customers were instructed to identify affected devices in inventory and return them to Pega Medical as soon as possible to address the issue. There returned devices can be returned via the FedEx information provided in the recall letter. Additionally customers were requested to provide the recall notification to all who need to be notified within your organization or any organization where the affected devices have been transferred. Contacts for questions include Mr. Enrique Garcia, at 450-688-5144 Ext 242, Email: [email protected] and Mr. Kildare Molina, at 450-688-5144 Ext. 267, Email: [email protected].

Distribution

Nationwide distribution to CA, FL, GA, HI, LA, MA, MO, NC, NY, OK. International distribution to AUSTRALIA, CANADA, DENMARK, GERMANY, ISRAEL, MEXICO, ROMANIA, RUSSIA, UNITED ARAB EMIRATES, UNITED KINGDOM

Quantity

31 devices