Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number Recalled by Pega Medical Inc. Due to The outer package label contained the incorrect length...
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
Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040(L)-SS. -Duval IM Telescopic System.
Quantity: 48
Why Was This Recalled?
The outer package label contained the incorrect length of the device. There is a label on the outer package and an additional label on the product contained in the package.
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