PAPR (Powered Air-Purifying Respirator) recall
PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1
Why was PAPR (Powered Air-Purifying Respirator) 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot code: JX20 (or week #20 of 2020)
- Product
- PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1
- Recalling firm
- Whirlpool Corporation
- Quantity
- 528 units
- Distribution
- The products were distributed to the following US states: MI.
- Recall date
- August 26, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)