Irwindale, CA, United States
WHPM Inc. recalls
1 recall recorded since 2018, most recently on 4 March 2022. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 4 March 2022
- Terminated
- 5 February 2025
- Reason
- Frm became aware that a customer complaint was reported to US FDA that SARS-CoV-2 Antigen Tests were sold domestically by a pharmacy in California. These Antigen Tests have not received FDA Emergency Use Authorization, nor have these tests been cleared or approved by FDA for commercial distribution in the U.S.
- Distribution
- U.S.: CA, FL, LA, MA and TX O.U.S.: N/A
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0892-2022
- First SIGN SARS-CoV-2 Antigen Test
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.