Device recall
Z-1624-2014: LATEX-FREE; T-U-R Y-Set; Nonvented Set for Transurethral Resection Procedures…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1624-2014 |
|---|---|
| Recall event | 68129 |
| Product | LATEX-FREE; T-U-R Y-Set; Nonvented Set for Transurethral Resection Procedures; 96 inch (244 cm); For Flexible Irrigation Container Systems; List No. 6543-01; single use; Hospira Product Usage: For use in transurethral resection procedures |
| Product code | GBX |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 6, 2016 |
| FEI number | 3013319212 |
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