Device recall
Z-0189-2007: Doc-U-Dose Prescription Management System, Item 8-PKIT. The product is packaged…
FDA device recall · Class II · Eatonform Inc
Key facts
| Recall number (Z-number) | Z-0189-2007 |
|---|---|
| Recall event | 36531 |
| Product | Doc-U-Dose Prescription Management System, Item 8-PKIT. The product is packaged and distributed in cartons. Each carton contains 1,000 sets of four packets or 4,000 individual packets per carton. |
| Product code | NQX |
| Recalling firm | Eatonform Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 21, 2012 |
| FEI number | 3005029365 |
At a glance
- None 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