Doral, FL, United States
Quest International, Inc. recalls
2 recalls recorded since 2018, most recently on 1 October 2025. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 1 October 2025
- Reason
- Due to distributing the measles IgG IVD without a premarket approved/cleared.
- Distribution
- All products were distributed in the United States. (Utah, Washington).
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0534-2026
- Brand Name: ReQuest Measles IgG Product Name: Rubeola IgG Enzyme Linked Immunoabsorbant Assay Model/Catalog Number: 01-190 Software Version: N/A Product Description: Measles IgG tests, performed using ELISA (Enzyme-L
Ongoing Class II Medical devices
- Recall started
- 17 July 2025
- Reason
- Measles IgM Test Kit lacks premarket approval or clearance.
- Distribution
- US Nationwide distribution in the states of Utah, Texas, and Arizona.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2552-2025
- Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM Model/Catalog Number: 01-190M Software Version: N/A Product Description: Measles IgM tests, performed using ELISA (Enzyme
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.