FDA Device recall Z-1834-2016
Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry
- FDA Device
- Class II
- terminated
- Published 2016-06-08
On 2016-06-08 the FDA classified a Class II recall of Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry by Microaire Surgical Instruments, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1834-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-11 |
| Published | 2016-06-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Microaire Surgical Instruments |
| Distribution | n/a |
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.
Identifiers
| code_info | 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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1834-2016%22
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