Facility
M D TECHNOLOGIES, INC.
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 1000139804 |
|---|---|
| Establishment type | Manufacture Medical Device |
| Location | 313 W. Sycamore St.. ELIZABETH, IL, US 61028 |
| Registration status | Active · expires 2026 |
| Parent company | M D TECHNOLOGIES, INC. (owner-operator 9009949) |
| Brand names | STH500; PT20 Trap |
Devices registered here (1)
- Trap, Sterile SpecimenProduct code BYZ · Class II · General Hospital · 21 CFR 880.6740
Recalls & enforcement
- Class IIOngoing2024-12-02Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-15. Verify this facility record at FDA →
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