KY Jelly Lubricant Recalled for Improper Storage Conditions
KY Jelly Lubricant 2 FL OZ (SKU 901443) distributed at Family Dollar stores was not stored in temperature-controlled areas. Consumers should discontinue use of product purchased between May–June 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 precautionary recall addresses improper storage conditions. No illnesses, injuries, or deaths have been reported. The hazard is theoretical, involving potential product degradation from temperature exposure.
Plain-English summary
KY Jelly Lubricant 2 FL OZ (SKU 901443) manufactured and distributed by Family Dollar Stores, Llc. is being recalled due to improper storage conditions.
The product was not appropriately stored in temperature-controlled areas between April 30, 2022 and June 10, 2022. Proper temperature control is necessary to maintain product integrity and safety.
The recall affects all units sold at Family Dollar retail stores nationwide between May 1 and June 10, 2022. Consumers who purchased this product during this timeframe should discontinue use.
Consumers with questions about this recall may contact Family Dollar Stores, Llc. or dispose of the product safely.
The recalled product
- Product
- KY JELLY LUBRICANT 2 FL OZ, SKU 901443
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Medical Device — Lubricant
- Hazard
- improper-storage
- temperature-control-failure
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