Recall Z-0793-2016— Smith & Nephew, Inc.
Class II · Terminated
Class II FDA medical device recall by Smith & Nephew, Inc., initiated 2016-01-11, terminated 2017-09-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.. Reason: Blade exhibiting fracture during hip arthroscopy procedures.
- Recalling firm
- Smith & Nephew, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-01-11
- Terminated
- 2017-09-18
- Firm location
- Andover, MA, United States
Product description
Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.
Reason for recall
Blade exhibiting fracture during hip arthroscopy procedures
Data sourced from openFDA. This site is unofficial and independent of the FDA.