Pregnancy Test 24ct recallZ-1184-2026 · Gold Star Distribution Inc · initiated Dec 26, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Gold Star Distribution Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Potential exposure of rodents and rodent activity in the distribution center.
FDA root cause category: Storage
What the company is doing
Gold Start Distribution, Inc. issued a press release on 12/26/2025 to notify the public of their recall of FDA regulated products due to the presence of rodent and avian contamination. The press release explained the risk to health, provided a list of retail outlets to which the products were distributed, and directed those in possession of the affected product to destroy them and verify such destruction by receipt provided to Gold Start at 1000 N. Humboldt Ave, Minneapolis, MN 55411. Refunds will be provided upon request. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products. If you have any questions, contact Gold Star at 612-617-9800, 7 days a week, 8:00 am to 5:00 pm, Central Standard Time. The firm followed with a letter to its consignees on 12/30/2025 via email with the same message.
Recall details
- Recall number
- Z-1184-2026
- Status
- Open, Classified
- Initiated by the company
- Dec 26, 2025
- Posted by the FDA
- Jan 27, 2026
- Recalling firm
- Gold Star Distribution Inc
- Product code
- LCX
- Distribution
- US Nationwide distribution in the states of Minnesota.
Product description
PREGNANCY TEST 24CT
Code information (models, lots, serial numbers)
UPC 048155920200
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Personal Care CassetteDelta Brands Inc. · Kit, Test, Pregnancy, Hcg, Over The Counter1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 98234).
- Z-1180-2026 · Open, ClassifiedBandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
- Z-1181-2026 · Open, ClassifiedCondoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GRE…
- Z-1182-2026 · Open, ClassifiedFeminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, A…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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