FDA Device recall Z-1328-2016
MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
- FDA Device
- Class II
- terminated
- Published 2016-04-13
On 2016-04-13 the FDA classified a Class II recall of MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device by Microaire Surgical Instruments, citing microAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del Vecchio French Rasp cannula), due to our receipt of three (3) complaints that it bent or broke during surge….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1328-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-08 |
| Published | 2016-04-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Microaire Surgical Instruments |
| Distribution | US |
Product
MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
Reason
MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del Vecchio French Rasp cannula), due to our receipt of three (3) complaints that it bent or broke during surgery. Accordingly, the PAL-R4011XL has also been put on production hold until further notice.
Identifiers
| code_info | Include lot numbers/serial numbers 0913228216, 0414243005, 0215266350, 0415269875, 0515271334 |
|---|
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-1328-2016%22
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