FDA recall Z-2815-2020

Whirlpool Corporation · Class II · device

Product

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.

Distribution

The products were distributed to the following US states: MI.

Key facts

Status
Terminated
Initiation date
2020-07-02
Report date
2020-08-26
Termination date
2021-06-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Benton Harbor, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2815-2020