Device recall
Z-2815-2020: PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1
FDA device recall · Class II · Whirlpool Corporation
Key facts
| Recall number (Z-number) | Z-2815-2020 |
|---|---|
| Recall event | 86034 |
| Product | PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1 |
| Product code | NZJ |
| Recalling firm | Whirlpool Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2021 |
| FEI number | 1826917 |
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