Device recall
Z-0292-2013: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin distributed by…
FDA device recall · Class I · Ethicon, Inc.
Key facts
| Recall number (Z-number) | Z-0292-2013 |
|---|---|
| Recall event | 63322 |
| Product | ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin distributed by ETHICON ETHICON Inc. Somerville, NJ 08876 USA Ref 2993 SURGIFLO Hemostatic Matrix, mixed with sterile saline or thrombin solution, is indicated for surgical procedures (except ophthalmic) for hemostasis, when control of… |
| Product code | LMF |
| Recalling firm | Ethicon, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 11, 2014 |
| PMA numbers | P990004 |
| FEI number | 2210968 |
At a glance
- None 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