Recall Z-2242-2021— Smith & Nephew Orthopaedics Ltd. (Aurora)
Class II · Terminated
Class II FDA medical device recall by Smith & Nephew Orthopaedics Ltd. (Aurora), initiated 2021-07-14, terminated 2024-05-13. FDA's recall record names no specific 510(k) clearance for this event. Product: smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery.. Reason: The nail head may become detached during surgery..
- Recalling firm
- Smith & Nephew Orthopaedics Ltd. (Aurora)
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-07-14
- Terminated
- 2024-05-13
- Firm location
- Leamington Spa, N/A, United Kingdom
Product description
smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery.
Reason for recall
The nail head may become detached during surgery.
Data sourced from openFDA. This site is unofficial and independent of the FDA.