Whirlpool Corporation
Benton Harbor, MI, US
Whirlpool Corporation appears in FDA device records in Benton Harbor, MI. FDA records list no 510(k) clearances, no PMA records and no registered establishments. As of , FDA records show one recall for this company.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 1
- Registered establishments
- 0
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
No FDA product codes recorded against this company.
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-2815-2020 | PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1 | 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. | Class II | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain