Reported Jun 8, 2016 · Terminated

Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry

MicroAire Surgical Instruments, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MicroAire Surgical Instruments, LLC · 3590 Grand Forks Blvd · Charlottesville, VA · 22911-9006

Is this the product you have?

  • Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry
Lot codes and dates
    • 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
Amount recalled
20 units

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 14, 2017 · Data as of Sep 19, 5:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.