FDA Medical devices recall ·
PREGNANCY TEST 24CT recall
- Recall number
- Z-1184-2026
- Date
- (initiated December 26, 2025)
- Company / brand
- Gold Star Distribution Inc
1000 Humboldt Ave N, Minneapolis, MN, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- N/A
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
PREGNANCY TEST 24CT
Why was it recalled?
Potential exposure of rodents and rodent activity in the distribution center.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UPC 048155920200
Distribution
US Nationwide distribution in the states of Minnesota.
States: Minnesota
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1184-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.