FDA Device recall Z-0107-2021
Ezycare Face Mask, Disposable Non Medical Face Masks - Product Usage: marketed under face mask umbrella EUA as source control
- FDA Device
- Class II
- ongoing
- Published 2020-10-21
On 2020-10-21 the FDA classified a Class II recall of Ezycare Face Mask, Disposable Non Medical Face Masks - Product Usage: marketed under face mask umbrella EUA as source control by Beyond White Spa D B A Ezywipe, citing disposable face masks labeled as non-medical were distributed to customers expecting medical use face masks.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0107-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-07-21 |
| Published | 2020-10-21 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Beyond White Spa D B A Ezywipe |
| Distribution | US |
Product
Ezycare Face Mask, Disposable Non Medical Face Masks - Product Usage: marketed under face mask umbrella EUA as source control.
Reason
Disposable face masks labeled as non-medical were distributed to customers expecting medical use face masks.
Identifiers
| code_info | Mfr. Lot No. EM20AP01, EM20AP02, EM20AP03, EM20MA01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0107-2021%22
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