Device recall
Z-2756-2011: Blake Silicone Drain, 1 unit, Manufactured for: Ethicon, Inc. Somerville, New…
FDA device recall · Class II · Ethicon, Inc.
Key facts
| Recall number (Z-number) | Z-2756-2011 |
|---|---|
| Recall event | 58335 |
| Product | Blake Silicone Drain, 1 unit, Manufactured for: Ethicon, Inc. Somerville, New Jersey, 08876-0151. Closed Wound Drainage Systems have been used as an adjunct in the following specialties to evacuate potentially detrimental collection of certain fluids (e.g. pus, extravascular blood, bile) from wounds… |
| Product code | KOG |
| Recalling firm | Ethicon, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 10, 2014 |
| 510(k) numbers | K953655 |
| FEI number | 2210968 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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