Device recall
Z-0972-2018: Vial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for…
FDA device recall · Class II · Medimop Medical Projects Ltd.
Key facts
| Recall number (Z-number) | Z-0972-2018 |
|---|---|
| Recall event | 79243 |
| Product | Vial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for use in healthcare facilities or in-home environment by the patient or care-giver to aid and support prescribed treatment and therapy. The device consists of the Vial2Bag piercing spike and cover, the IV Port connector… |
| Product code | LHI |
| Recalling firm | Medimop Medical Projects Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 23, 2024 |
| 510(k) numbers | K140730 |
| FEI number | 3000223297 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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