Recall Z-1241-2017— Smith & Nephew, Inc.
Class II · Terminated
Class II FDA medical device recall by Smith & Nephew, Inc., initiated 2017-02-02, terminated 2019-09-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703. Reason: The single use devices are provided sterile and do not have an expiration date on the label..
- Recalling firm
- Smith & Nephew, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-02-02
- Terminated
- 2019-09-20
- Firm location
- Memphis, TN, United States
Product description
Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703
Reason for recall
The single use devices are provided sterile and do not have an expiration date on the label.
Data sourced from openFDA. This site is unofficial and independent of the FDA.