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Terminated

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

FDA Recall Z-0270-2020 · Posted None

Recalling FirmPega Medical Inc.
Recall StatusTerminated
Product CodeLXH
Date Initiated2019-10-02
Date Terminated2020-10-26
Product Quantity31 devices

Reason for Recall

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

Firm 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].

Root Cause

Device Design

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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