PlainRecalls
FDA Devices Moderate Class II Terminated

PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1

Reported: August 26, 2020 Initiated: July 2, 2020 #Z-2815-2020

Product Description

PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1

Reason for Recall

The rivets that secure the elastic headband to the face shield have the potential to be mis-assembled. When this condition occurs, it can result in a headband that can become loose from face shield allowing the face shield to shield on the user.

Details

Recalling Firm
Whirlpool Corporation
Units Affected
528 units
Distribution
The products were distributed to the following US states: MI.
Location
Benton Harbor, MI

Frequently Asked Questions

What product was recalled?
PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1. Recalled by Whirlpool Corporation. Units affected: 528 units.
Why was this product recalled?
The rivets that secure the elastic headband to the face shield have the potential to be mis-assembled. When this condition occurs, it can result in a headband that can become loose from face shield allowing the face shield to shield on the user.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 26, 2020. Severity: Moderate. Recall number: Z-2815-2020.