Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE Recalled by Pega Medical Inc. Due to SCFE Drivers of the Free-Gliding SCFE Screw System...
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
Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE Screw System with catalogue number SCF-MLD265 and SCF-MLD273.
Quantity: 4 units
Why Was This Recalled?
SCFE Drivers of the Free-Gliding SCFE Screw System are recalled because the handle of the instruments may detach from the shaft if high torques are applied in counter-clockwise rotation.
Where Was This Sold?
This product was distributed to 2 states: FL, TN
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