SeraQuest MEAS GRecalls & reported problems
Quest International, Inc. · Measles virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Oct 1, 2025Open, Classified
Due to distributing the measles IgG IVD without a premarket approved/cleared.
Z-0534-2026 · Root cause: No Marketing Application · FDA record ↗
Other Enzyme Linked Immunoabsorbent Assay, Rubeola Igg devices
- VIDAS® Measles IgG 30219Biomerieux SA · Enzyme linked immunoabsorbent assay, rubeola IgG2 recalls17 reports
- ReQuest MEAS MQuest International, Inc. · Enzyme Linked Immunoabsorbent Assay, Rubeola Igg1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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