Recall Z-0406-2018— Smith & Nephew, Inc.
Class II · Terminated
Class II FDA medical device recall by Smith & Nephew, Inc., initiated 2017-10-23, terminated 2018-08-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Radial Osteotome Blade, REF 71369314. Used for cutting or preparing bone.. Reason: The expiration date provided on the label is incorrect..
- Recalling firm
- Smith & Nephew, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-10-23
- Terminated
- 2018-08-24
- Firm location
- Memphis, TN, United States
Product description
Radial Osteotome Blade, REF 71369314. Used for cutting or preparing bone.
Reason for recall
The expiration date provided on the label is incorrect.
Data sourced from openFDA. This site is unofficial and independent of the FDA.