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Terminated

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

FDA Recall Z-2815-2020 · Posted None

Recalling FirmWhirlpool Corporation
Recall StatusTerminated
Product CodeNZJ
Date Initiated2020-07-02
Date Terminated2021-06-25
Product Quantity528 units

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.

Firm Action

Customers were contacted via email/telephone beginning 6/18/20. Rework was conducted in-house at the customer facilities.

Root Cause

Manufacturing material removal

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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