Device recall
Z-2059-2019: Zyno Medical Administration Set -105"ADMIN SET 20DP W/FILTER 2YSITES CLMP- For…
FDA device recall · Class II · Zyno Medical LLC
Key facts
| Recall number (Z-number) | Z-2059-2019 |
|---|---|
| Recall event | 83026 |
| Product | Zyno Medical Administration Set -105"ADMIN SET 20DP W/FILTER 2YSITES CLMP- For Use with Zyno Medical Infusion pumps or Gravity Feed Product Code: B2-70072-F |
| Product code | FPA |
| Recalling firm | Zyno Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 22, 2020 |
| 510(k) numbers | K132841 |
| FEI number | 3006575795 |
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