First Response 2-Count Pregnancy Test Recalled for Improper Storage
Family Dollar Stores is recalling First Response 2 CT pregnancy tests due to improper storage outside temperature-controlled areas. Affected products were sold nationwide between May 1 and June 10, 2022.
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: This FDA Class II voluntary precautionary recall involves improper storage conditions that could affect device performance. No failures, inaccuracies, or injuries have been reported, and the hazard is operational rather than an inherent product defect.
Plain-English summary
Family Dollar Stores, LLC is recalling First Response 2 CT pregnancy tests (SKU 902343) distributed to Family Dollar retail stores nationwide. Approximately 77 units were affected.
The product was not appropriately stored in temperature-controlled areas between April 30 and June 10, 2022. Improper storage conditions may affect the reliability and performance of the medical device.
The recalled product was sold to consumers between May 1 and June 10, 2022. If you purchased this product during this timeframe at Family Dollar, consult the retailer or manufacturer for further guidance.
The recalled product
- Product
- FIRST RESPONSE 2 CT, SKU 902343
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Medical Device — Pregnancy Test
- Hazard
- improper-storage
- temperature-control
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
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03
- SevereAbiomed Automated Impella Controller recalled for motor control and pump failure risks
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- CriticalMedline spinal anesthetic kits recalled for quality and efficacy concerns
FDA (Devices) · 2026-06-03
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03