Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PATH(R) THREAD CUP ADAPTOR Recalled by Microport Orthopedics INC. Due to Difficulty removing the cup adaptor from the impaction...
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 Microport Orthopedics INC. directly.
Affected Products
PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.
Quantity: 140 units
Why Was This Recalled?
Difficulty removing the cup adaptor from the impaction handle during surgery
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Microport Orthopedics INC.
Microport Orthopedics INC. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report