Device recall
Z-0319-2007: RYM-5000 InVision-Plus Neutral Displacement I.V. Connector, packaged 200 units…
FDA device recall · Class II · Rymed Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0319-2007 |
|---|---|
| Recall event | 36854 |
| Product | RYM-5000 InVision-Plus Neutral Displacement I.V. Connector, packaged 200 units per box, 5 boxes per case (1000 units/case); labeled as Sterile-Nonpyrogenic; assembled in Mexico for Rymed Technologies, Inc., Austin, TX. |
| Product code | FPA |
| Recalling firm | Rymed Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 26, 2007 |
| 510(k) numbers | K991653 |
| FEI number | 3005951712 |
At a glance
- 1–9 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