FDA Device recall Z-1407-2017
MicroAire K-Wires
- FDA Device
- Class II
- terminated
- Published 2017-03-15
On 2017-03-15 the FDA classified a Class II recall of MicroAire K-Wires by Microaire Surgical Instruments, citing mislabeling on three lots of K-Wires. The incorrect product description " dual trocar" instead of "single trocar" was on the product label on the following parts: 1600-9355NS (lot….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1407-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-21 |
| Published | 2017-03-15 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Microaire Surgical Instruments |
| Distribution | n/a |
Product
MicroAire K-Wires
Reason
Mislabeling on three lots of K-Wires. The incorrect product description " dual trocar" instead of "single trocar" was on the product label on the following parts: 1600-9355NS (lot 61005), 1600-9625NS (lot 60297), and 1604-162NS (lot 62856).
Identifiers
| code_info | Part Number, Lot Number, Quantity Distributed to Field 1600-9355NS, 61005, 56; 1600-9625NS, 60297, 209; 1604-162NS, 62856, 97. |
|---|
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-1407-2017%22
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