Device recall
Z-0922-03: ThinPrep Microscope Slides for Non-Gynecologic Use Size 1'' x 3'' Reorder…
FDA device recall · Class III · Cytyc Corporation
Key facts
| Recall number (Z-number) | Z-0922-03 |
|---|---|
| Recall event | 25529 |
| Product | ThinPrep Microscope Slides for Non-Gynecologic Use Size 1'' x 3'' Reorder Number: 70214-001 |
| Product code | KEW |
| Recalling firm | Cytyc Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 22, 2003 |
| FEI number | 1000120743 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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