FDA DevicesClass II
PREGNANCY TEST 24CT
Published: February 4, 2026Recall ID: Z-1184-2026Category: devicesCountry: US
Reason for Recall / Hazard
Potential exposure of rodents and rodent activity in the distribution center.
Product Description & Identification
PREGNANCY TEST 24CT
Affected Products
PREGNANCY TEST 24CT
Additional Source Details
| Field | Value |
|---|---|
| City | Minneapolis |
| State | MN |
| Event id | 98234 |
| Address 1 | 1000 Humboldt Ave N |
| Address 2 | N/A |
| Code info | UPC 048155920200 |
| Postal code | 55411-3964 |
| Report date | 20260204 |
| Product type | Devices |
| Product quantity | N/A |
| Reason for recall | Potential exposure of rodents and rodent activity in the distribution center. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251226 |
| Initial firm notification | Press Release |
| Center classification date | 20260127 |
Overview
- Recalling FirmGOLD STAR DISTRIBUTION INC
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the states of Minnesota.