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.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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
- Affected units
- 5
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.
Part of a larger recall action
This product is one of 22 recalled by Family Dollar Stores, Llc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 22 products in this recall →Related recalls
Same manufacturer · Family Dollar Stores, Llc.
See all →- ModerateFamily Dollar marijuana test strips recalled over improper storage
FDA (Devices) · 2023-11-15
- HighFamily Dollar Pregnancy Test Recalled Due to Improper Storage Conditions
FDA (Devices) · 2023-11-15
- ModerateFirst Response 2 CT Recalled for Improper Temperature Storage
FDA (Devices) · 2023-11-15
- ModerateFixodent Denture Cream Recalled Due to Improper Storage Conditions
FDA (Devices) · 2023-11-15
- ModerateOral B Mouth Sore Rinse Recall Due to Improper Storage Conditions
FDA (Devices) · 2023-11-15
Same hazard · improper storage
See all →- ModerateFairhope Cold Brew Coffee Concentrate Recall Over Missing Refrigeration Label
FDA (Food) · 2026-06-24
- ModerateOrtho Clinical Diagnostics Total Bili-Alkp XT Reagent Recall
FDA (Devices) · 2025-06-04
- ModerateHemoCue HemoTrol High Control Product Recalled Due to Storage Conditions
FDA (Devices) · 2025-06-04
- ModerateAbbott Rapid DX Multi Analyte Control Affected by Storage Temperature Excursion
FDA (Devices) · 2025-06-04
- ModerateAbbott Diagnostics HIV Combo Calibrator Affected by Cold Chain Exposure
FDA (Devices) · 2025-06-04
Similar recalls
- HighMIRALAX 8.3 OZ Recalled Due to Improper Storage Temperature Conditions
FDA (Drugs) · 2022-08-31
- HighPetroleum Jelly Products Recalled for Improper Storage Conditions
FDA (Drugs) · 2022-08-31
- HighVicks DayQuil NyQuil Combination Pack Recalled for Storage Temperature
FDA (Drugs) · 2022-08-31
- ModerateOrajel Non Med Teething Gel Recalled for Improper Storage Conditions
FDA (Drugs) · 2022-08-31
- HighAntifungal Cream Recalled for Improper Storage Temperature Conditions
FDA (Drugs) · 2022-08-31
- ModerateBenadryl Extra Strength Cream Recalled for Improper Storage Conditions
FDA (Drugs) · 2022-08-31