Facility
BIOMERICA DE MEXICO, S.A. DE C.V.
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 3004569406 |
|---|---|
| Establishment type | Manufacture Medical Device |
| Location | SATURNO 20-A MEXICALI Baja California, MX 21210 |
| Registration status | Active · expires 2026 |
| Parent company | Biomerica, Inc. (owner-operator 2016793) |
| Brand names | Shigella Lateral Flow Rapid Test |
Devices registered here (1)
- Antisera, All Types, Shigella Spp.Product code GNB · Class II · Microbiology · 21 CFR 866.3660
Recalls & enforcement
- Class IITerminated2014-09-18A potential issue with false high values.
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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