Device recall
Z-0555-2019: Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product…
FDA device recall · Class II · Pfizer Inc.
Key facts
| Recall number (Z-number) | Z-0555-2019 |
|---|---|
| Recall event | 81178 |
| Product | Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary relief of minor menstrual cramp pain and associated back aches. |
| Product code | IMD |
| Recalling firm | Pfizer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2023 |
| FEI number | 2416101 |
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