Recall Z-1834-2016— MicroAire Surgical Instruments, LLC
Class II · Terminated
Class II FDA medical device recall by MicroAire Surgical Instruments, LLC, initiated 2016-03-11, terminated 2017-02-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry. Reason: MicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end users and were missing the lock and unlock symbol markings on them..
- Recalling firm
- MicroAire Surgical Instruments, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-03-11
- Terminated
- 2017-02-14
- Firm location
- Charlottesville, VA, United States
Product description
Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry
Reason for recall
MicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end users and were missing the lock and unlock symbol markings on them.
Data sourced from openFDA. This site is unofficial and independent of the FDA.