Device recall
Z-1217-2010: Live Better 1cc, 31 gauge x 5/16 inch U-100 Insulin Syringe short needle. 100…
FDA device recall · Class II · Ulti Med, Inc.
Key facts
| Recall number (Z-number) | Z-1217-2010 |
|---|---|
| Recall event | 54655 |
| Product | Live Better 1cc, 31 gauge x 5/16 inch U-100 Insulin Syringe short needle. 100 syringes, Manufactured by UltiCare. Used to draw a quantity of pharmaceutical from its container and allow administration of the pharmaceutical directly to the patient. As an alternative use the product will allow… |
| Product code | FMF |
| Recalling firm | Ulti Med, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2011 |
| 510(k) numbers | K062702 |
| FEI number | 2183771 |
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