Device recall
Z-1496-2019: ThermaCare HEATWRAPS, ADVANCED BACK PAIN THERAPY, SKU: a) F00573301020A b)…
FDA device recall · Class II · PF Consumer Healthcare 1 LLC
Key facts
| Recall number (Z-number) | Z-1496-2019 |
|---|---|
| Recall event | 82781 |
| Product | ThermaCare HEATWRAPS, ADVANCED BACK PAIN THERAPY, SKU: a) F00573301020A b) F00573301026X c) F00573301009B Product Usage: ThermaCare(R) HeatWraps are indicated in adults to provide heat therapy for the temporary relief of minor muscular and joint pains associated with overexertion, strains, sprains… |
| Product code | IMD |
| Recalling firm | PF Consumer Healthcare 1 LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2024 |
| FEI number | 3007593958 |
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