Device recall
Z-0675-2016: InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable…
FDA device recall · Class II · Rymed Technologies, LLC
Key facts
| Recall number (Z-number) | Z-0675-2016 |
|---|---|
| Recall event | 72997 |
| Product | InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use. |
| Product code | FPA |
| Recalling firm | Rymed Technologies, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 19, 2016 |
| 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