Device recall
Z-0861-2016: Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-0861-2016 |
|---|---|
| Recall event | 73168 |
| Product | Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001 InVision-Plus Needless IV Connectors are used for single patient use in IV and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries… |
| Product code | FPA |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 19, 2016 |
| FEI number | 3008403546 |
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