Device recall
Z-0934-03: T-U-R Y-Set Non-Vented Set for Transurethral Resection Procedures For Use with…
FDA device recall · Class II · Abbott Laboratories HPD/ADD
Key facts
| Recall number (Z-number) | Z-0934-03 |
|---|---|
| Recall event | 26348 |
| Product | T-U-R Y-Set Non-Vented Set for Transurethral Resection Procedures For Use with Flexible Irrigation Container System, 84 inch (213 cm) Nominal Length, No. 15252-02; Made in Costa Rica, Abbott Laboratories, North Chicago, IL 60064 |
| Product code | FPA |
| Recalling firm | Abbott Laboratories HPD/ADD |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 20, 2003 |
| FEI number | 1415939 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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