Device recall
Z-0556-2019: Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS; MUSCLE PAIN THERAPY, 3…
FDA device recall · Class II · Pfizer Inc.
Key facts
| Recall number (Z-number) | Z-0556-2019 |
|---|---|
| Recall event | 81178 |
| Product | Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS; MUSCLE PAIN THERAPY, 3 HEATWRAPS a) UPC 0573301311 b) UPC 0573301311 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and arthritis. |
| 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