Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega Medical Inc. Due to There is a potential for the screws to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pega Medical Inc. directly.
Affected Products
SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery
Quantity: 31 devices
Why Was This Recalled?
There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pega Medical Inc.
Pega Medical Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report