VeriQuick Pregnancy Tests Recalled Due to Improper Storage
Family Dollar is recalling VeriQuick pregnancy tests that were not stored in temperature-controlled areas between April-June 2022. Improper storage conditions may affect test accuracy.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II device recall with theoretical risk to test accuracy due to improper temperature storage. No reported incidents of test failures, inaccuracies, or harm to users.
Plain-English summary
Family Dollar Stores, LLC is recalling VeriQuick Pregnancy Test 1CT (SKUs 901260 and 939504) for improper storage. Approximately 22,062 units of SKU 901260 and 118 units of SKU 939504 were affected.
The recalled products were not stored in temperature-controlled areas from April 30, 2022 through June 10, 2022. Temperature fluctuations can compromise the reliability and accuracy of pregnancy test results.
The affected products were distributed to Family Dollar retail stores nationwide and sold between May 1, 2022 and June 10, 2022. Consumers who purchased these products during this period should verify the SKU and inspect the product packaging.
The recalled product
- Product
- VERIQUICK PREGNANCY TEST 1CT, SKU 901260, 939504
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Medical Device — Diagnostic Test
- Hazard
- improper-storage
- accuracy-degradation
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All product sold between May 1
- 2022 - June 10
- 2022.
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighPhilips Azurion X-Ray Systems Table Movement Control Defect Recall
FDA (Devices) · 2026-05-27
- HighAzurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula Cardiopulmonary Bypass Catheter Recall
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula cardiopulmonary bypass catheter
FDA (Devices) · 2026-05-27
- HighTangent Single Use Digital Catheter Recalled for Distal Shaft Fractures
FDA (Devices) · 2026-05-27