Drug recall
MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
FDA recall event 73373 · Class II · MicroAire Surgical Instruments, LLC
Key facts
| Event ID | 73373 |
|---|---|
| Recall numbers | Z-1328-2016 |
| Recalling firm | MicroAire Surgical Instruments, LLC |
| Product type | Devices |
| Products | MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Feb 8, 2016 |
| Report date | Apr 13, 2016 |
| Termination date | Feb 14, 2017 |
| City | Charlottesville |
| State | VA |
| Country | United States |
| FEI number | 2020601 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: