Device recall
Z-2340-2008: FloSeal Endoscopic Applicator, Product Code 1500181. The product is indicated…
FDA device recall · Class II · Baxter Bioscience
Key facts
| Recall number (Z-number) | Z-2340-2008 |
|---|---|
| Recall event | 49104 |
| Product | FloSeal Endoscopic Applicator , Product Code 1500181. The product is indicated in surgical procedures (other than in neurosurgical, opthalmic, and urological) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical. |
| Product code | LMF |
| Recalling firm | Baxter Bioscience |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 11, 2011 |
| PMA numbers | P990009 |
| FEI number | 1417572 |
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