Device recall
Z-1319-2013: Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit…
FDA device recall · Class II · Summit Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1319-2013 |
|---|---|
| Recall event | 65034 |
| Product | Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit Medical, Inc., 815 Northwest Parkway, Suite 100, St. Paul, MN 55121 Use to make an incision in the tympanic membrane. |
| Product code | JYO |
| Recalling firm | Summit Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2013 |
| FEI number | 3008719017 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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