Z-1184-2026 Class II Ongoing

Recalled by GOLD STAR DISTRIBUTION INC — Minneapolis, MN

FDA device recall Z-1184-2026 was initiated by GOLD STAR DISTRIBUTION INC on December 26, 2025 and is designated Class II. Reason for recall: Potential exposure of rodents and rodent activity in the distribution center. The recall status is ongoing. Affected quantity: N/A.

Recall Details

Product Type
Devices
Report Date
February 4, 2026
Initiation Date
December 26, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

PREGNANCY TEST 24CT

Reason for Recall

Potential exposure of rodents and rodent activity in the distribution center.

Distribution Pattern

US Nationwide distribution in the states of Minnesota.

Code Information

UPC 048155920200