Recall Z-1712-2014— Microport Orthopedics INC.
Class II · Terminated
Class II FDA medical device recall by Microport Orthopedics INC., initiated 2014-04-30, terminated 2014-12-01. FDA's recall record names no specific 510(k) clearance for this event. Product: PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.. Reason: Difficulty removing the cup adaptor from the impaction handle during surgery.
- Recalling firm
- Microport Orthopedics INC.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-04-30
- Terminated
- 2014-12-01
- Firm location
- Arlington, TN, United States
Product description
PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.
Reason for recall
Difficulty removing the cup adaptor from the impaction handle during surgery
Data sourced from openFDA. This site is unofficial and independent of the FDA.