Device recall
Z-2753-2011: Bariatric Target Ring (Nitinol) (a thin, circular nitinol ring) Model #…
FDA device recall · Class II · Kapp Surgical Instrument Inc
Key facts
| Recall number (Z-number) | Z-2753-2011 |
|---|---|
| Recall event | 59024 |
| Product | Bariatric Target Ring (Nitinol) (a thin, circular nitinol ring) Model # K-9536-N, Lot #08-001, Lot #08-002 & Lot #08-003. One ring per plastic pouch, three rings are then placed into a plastic box with lid. This box is then placed into a solid white box. Item is shipped and sold non-sterile. It is… |
| Product code | NEU |
| Recalling firm | Kapp Surgical Instrument Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 19, 2013 |
| 510(k) numbers | K072216 |
| FEI number | 1522875 |
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