Device recall
Z-1780-2018: EasyTouch (ET) Insulin Syringe 29G 0.5ml " (Item 829555) Product Usage: INTENDED…
FDA device recall · Class II · MHC Medical Products LLC
Key facts
| Recall number (Z-number) | Z-1780-2018 |
|---|---|
| Recall event | 79950 |
| Product | EasyTouch (ET) Insulin Syringe 29G 0.5ml " (Item 829555) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY |
| Product code | FMI |
| Recalling firm | MHC Medical Products LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K112789 |
| FEI number | 3005798905 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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