Pneumatic Impactor recall
Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry
Why was Pneumatic Impactor recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
2500-100 Ser#s 1547,1546,1545,1544, 1543,1542, 1541,1540,1539,1538,1537,1536,1535,1534,1533,1532 2500-200 Ser#s 1464,1463,1462,1461
- Product
- Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry
- Recalling firm
- MicroAire Surgical Instruments, LLC
- Quantity
- 20 units
- Distribution
- United States
- Recall date
- June 8, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)