Device recall
Z-0428-2007: Taut Intraducer Peritoneal Catheter, 12 Fr x 10 Fr x 20.3 cm; a sterile, Rx…
FDA device recall · Class II · Taut, Inc.
Key facts
| Recall number (Z-number) | Z-0428-2007 |
|---|---|
| Recall event | 37182 |
| Product | Taut Intraducer Peritoneal Catheter, 12 Fr x 10 Fr x 20.3 cm; a sterile, Rx peritoneal catheter for single use, individually packaged in a Tyvek/clear pouch; Taut Inc., 2561 Kaneville Ct., Geneva, IL 60134; the individually packaged, sterilirzed catheter was sold in two configurations: a) catalog… |
| Product code | GBW |
| Recalling firm | Taut, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2009 |
| 510(k) numbers | K960883 |
| FEI number | 1419305 |
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