Device recall
Z-1103-2010: NIPRO, GLUCOPRO INSULIN SYRINGES, SINGLE USE INSULIN SYRINGE with needle, 1CC…
FDA device recall · Class II · Nipro Medical Corporation
Key facts
| Recall number (Z-number) | Z-1103-2010 |
|---|---|
| Recall event | 54358 |
| Product | NIPRO, GLUCOPRO INSULIN SYRINGES, SINGLE USE INSULIN SYRINGE with needle, 1CC 30g 5/16", U-100 INSULIN, LATEX FREE. Distributed by: NIPRO MEDICAL CORPORATION 3150 N.W. 107th Ave., Miami, Florida 33172. Packaged 10 syringes in a pouch, 10 pouches in a box (100 pieces), 5 boxes in a case (500 pieces)… |
| Product code | FMF |
| Recalling firm | Nipro Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2010 |
| FEI number | 1000132332 |
At a glance
- None 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