Home › MONOBIND, INC. › T4 AccuBind ELISA Test System - 960 Wells
T4 AccuBind ELISA Test System - 960 Wells
MONOBIND, INC. · Model 225-300 · UDI-DI 00816870021683
CDX
Prescription
1
510(k) clearances
100
Adverse events
1
Recalls
13
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-04 | DRG International, Inc. | An incoming complaint reported that the expiration date on the kit box label and Certificate of Analysis (CoA) exceeded the shelf life of the standards and control solutions in the |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.