Device recall
Z-0027-05: Uterine Introducing Catheter 5F, 300 mm in length. The product is shipped in a…
FDA device recall · Class II · Bioteque America Inc
Key facts
| Recall number (Z-number) | Z-0027-05 |
|---|---|
| Recall event | 31276 |
| Product | Uterine Introducing Catheter 5F, 300 mm in length. The product is shipped in a sterile tyvek pouch |
| Recalling firm | Bioteque America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 14, 2005 |
| FEI number | 1000121341 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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