Polident Denture Cleansers Recalled Due to Improper Storage
Polident denture cleansers sold at Family Dollar stores nationwide are being recalled due to improper storage conditions. No illnesses or injuries have been reported.
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 recall with no reported illnesses or injuries. The hazard from improper temperature storage is theoretical and precautionary, meeting the criteria for Moderate severity per the rubric.
Plain-English summary
Family Dollar Stores, LLC is recalling Polident denture cleansers distributed to Family Dollar retail locations nationwide. The affected products (84 CT, SKU 901634 and 28 CT, SKU 906131) were not appropriately stored in temperature-controlled areas.
Products sold between May 1 and June 10, 2022 are affected by the recall. The improper storage conditions occurred between April 30 and June 10, 2022.
No illnesses or injuries have been reported in connection with this recall. This is an FDA Class II recall.
The recalled product
- Product
- POLIDENT DENTURE CLEANSERS 84 CT, SKU 901634 POLIDENT DENTURE CLNS TAB 28CT, SKU 906131
- Manufacturer
- Family Dollar Stores, Llc.
- Hazard
- Affected units
- 34
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