Antibacterial Wipes Recalled for Improper Storage Conditions
Family Dollar Stores recalls Disney Licensed Anti Bac Wipes and Antibacterial Wipes due to storage temperature deviations. The products were distributed nationwide to Family Dollar stores from April 30 through June 10, 2022.
The agency’s classification
FDA (Drugs): 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 is a Class II FDA recall with no reported illnesses or injuries documented in the available source material. The hazard—improper storage temperature conditions—represents a potential precautionary issue rather than demonstrated safety harm. Per the severity rubric, Class II recalls without reported incidents are classified as Moderate.
Plain-English summary
Family Dollar Stores, LLC is recalling Disney Licensed Anti Bac Wipes (SKU 998908, 20 count) and Antibacterial Wipes (SKU 2007538, 40 count).
The products were distributed to Family Dollar stores nationwide between April 30, 2022 and June 10, 2022.
The recall was issued because these products were held outside appropriate storage temperature conditions, which constitutes a Current Good Manufacturing Practice (CGMP) deviation. This storage deviation may affect product quality and efficacy.
The recalled product
- Product
- DISNEY LICENSED ANTI BAC WIPES 20 CT SKU 998908; ANTIBACTERIAL WIPES 40CT SKU 2007538 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Drug — Antimicrobial Wipes
- 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 (2)
- SKUs: 998908
- 2007538
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
Similar recalls
- HighSimply Saline Nasal Mist Recalled for Improper Storage Conditions
FDA (Devices) · 2022-08-24
- HighSkin liquid bandage recalled for improper temperature storage
FDA (Devices) · 2022-08-24
- ModeratePolident Denture Cleansers Recalled Due to Improper Storage
FDA (Devices) · 2022-08-24
- HighGS Saline Solution recalled due to improper temperature storage
FDA (Devices) · 2022-08-24
- ModerateKY Jelly Lubricant Recalled for Improper Storage Conditions
FDA (Devices) · 2022-08-24
- ModerateSkincare Product Recalled for Temperature Storage Deviation
FDA (Drugs) · 2022-06-08