Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0270-2020 — SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery

U.S. FDA — Device Enforcement · Canada · 2019-10-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0270-2020
Date of alert
2019-10-02
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Pega Medical Inc.
Product category
device
Product type
Devices
Reported risk: There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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