← FDA ENFORCEMENT
Z-1184-2026Class II
GOLD STAR DISTRIBUTION INC
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
GOLD STAR DISTRIBUTION INC
Product type
Device
Status
Ongoing
Report date
2026-02-04
Distribution
US Nationwide distribution in the states of Minnesota.
Firm state
MN
Product quantity
N/A
Initiated by
Voluntary: Firm initiated
Reason for recall
Potential exposure of rodents and rodent activity in the distribution center.
Product description
PREGNANCY TEST 24CT
Code / lot info
UPC 048155920200
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →