Recall Z-1184-2026— GOLD STAR DISTRIBUTION INC
Class II · Ongoing
Class II FDA medical device recall by GOLD STAR DISTRIBUTION INC, initiated 2025-12-26. FDA's recall record names no specific 510(k) clearance for this event. Product: PREGNANCY TEST 24CT. Reason: Potential exposure of rodents and rodent activity in the distribution center..
- Recalling firm
- GOLD STAR DISTRIBUTION INC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-12-26
- Firm location
- Minneapolis, MN, United States
Product description
PREGNANCY TEST 24CT
Reason for recall
Potential exposure of rodents and rodent activity in the distribution center.
Data sourced from openFDA. This site is unofficial and independent of the FDA.