Dial Men's Eucalyptus Body Wash Recalled Due to Storage Temperature Deviation
Family Dollar Stores is recalling Dial Men's Eucalyptus Body Wash 20 fl oz due to improper storage temperature conditions during distribution.
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 involving a manufacturing compliance deviation with no reported illnesses, injuries, or confirmed contamination. The recall appears precautionary based on improper storage conditions rather than confirmed product harm.
Plain-English summary
Family Dollar Stores, Llc. is recalling Dial Men's Eucalyptus AB Body Wash (20 fl oz, SKU 2096030) that was distributed to specific Family Dollar Stores nationwide between April 30, 2022 and June 10, 2022. The recall was initiated due to a Current Good Manufacturing Practice (CGMP) deviation: the product was held outside appropriate storage temperature conditions.
If you purchased this recalled product, discontinue use and return it to the point of purchase for a refund or replacement. For additional information, contact Family Dollar Stores, Llc. or the FDA.
The recalled product
- Product
- DIAL MENS EUCALYPTUS AB BODY WASH 20 FLOZ SKU 2096030 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
- Manufacturer
- Family Dollar Stores, Llc.
- Hazard
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 (1)
- SKU: 2096030
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 100 recalled by Family Dollar Stores, Llc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 100 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