Pneumatic Impactor — Class II medical device recall Z-1834-2016
Terminated recall by MicroAire Surgical Instruments, LLC, reported 2016-06-08. MicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end
| Recall number | Z-1834-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MicroAire Surgical Instruments, LLC, Charlottesville, VA, United States |
| Recall initiated | 2016-03-11 |
| Classified | 2016-05-27 |
| Reported by FDA | 2016-06-08 |
| Terminated | 2017-02-14 |
| Quantity | 20 units |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1834-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.