Device recall
Z-2158-2013: Steinmann Pin, packed in a clear tube with end caps, tubes packed in a sterile…
FDA device recall · Class II · MicroAire Surgical Instruments, LLC
Key facts
| Recall number (Z-number) | Z-2158-2013 |
|---|---|
| Recall event | 66029 |
| Product | Steinmann Pin, packed in a clear tube with end caps, tubes packed in a sterile barrier pouch, 6 pouches/sales unit. Pouches are labeled in part ***MicroAire Surgical Instruments 3590 Grand Forks Blvd Charlottesville, VA LLC 22911*** Models: 1620-109 1636-509 1620-509 1640-509 1620-609 1648-509… |
| Product code | HTY |
| Recalling firm | MicroAire Surgical Instruments, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2014 |
| 510(k) numbers | K863764 |
| FEI number | 2020601 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database