Device recall
Z-0150-04: Konica Minolta Duplicating Film Emulsions. Konica Medical Film. Emulsion numbers…
FDA device recall · Class III · Konica Medical Imaging, Inc.
Key facts
| Recall number (Z-number) | Z-0150-04 |
|---|---|
| Recall event | 27488 |
| Product | Konica Minolta Duplicating Film Emulsions. Konica Medical Film. Emulsion numbers X(=any number), X 742, X842, X152. Film type SR-DUP 8x10, 10x12, 11x14, and 14x17. Film type PPD DUP 10x12 only and Emulsion Number X152. SR-DUP C 14x17 Emulsion X023 only. |
| Product code | IWZ |
| Recalling firm | Konica Medical Imaging, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 29, 2004 |
| FEI number | 2241281 |
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