Device recall
Z-0622-2011: ThermaCare Menstrual 8 Hour Heat Wraps, 3 count, NDC 0573-3020-02, SKU: 302002…
FDA device recall · Class II · Pfizer Global
Key facts
| Recall number (Z-number) | Z-0622-2011 |
|---|---|
| Recall event | 56855 |
| Product | ThermaCare Menstrual 8 Hour Heat Wraps, 3 count, NDC 0573-3020-02, SKU: 302002, UPC: 3-0573-3020-02-9, Wyeth Consumer Healthcare, P.O. Box 26609, Richmond, VA 23261-6609 |
| Product code | IMD |
| Recalling firm | Pfizer Global |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2011 |
| FEI number | 3008678286 |
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