QP Cold Multi-Symptom medication recalled for improper storage conditions
Family Dollar Stores is recalling QP Cold Multi-Symptom Day/Night medication distributed April 30–June 10, 2022, to select stores because the product was held at incorrect temperatures. Consumers should return the product to the store for a refund.
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 is a Class II pharmaceutical recall with no reported illnesses, injuries, or deaths. The hazard is improper storage temperature, a CGMP compliance and quality control issue rather than a high-risk pathogen or allergen. The recall is precautionary in nature.
Plain-English summary
Family Dollar Stores, Llc. is recalling QP Cold Multi-Symptom Day/Night Complete 24-count medication (SKU: 916058) that was distributed to select Family Dollar Stores between April 30, 2022, and June 10, 2022.
The product is being recalled because it was held outside appropriate storage temperature conditions, which constitutes a deviation from Current Good Manufacturing Practice (CGMP) standards.
The affected product was distributed to specific Family Dollar Stores nationwide during the recall period.
Consumers who purchased this medication should stop using it and return it to the store where it was purchased for a refund.
The recalled product
- Product
- QP COLD MULTI SYMPTM DAY NITE CPLT 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Drug — Cold Medication
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: 916058
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 →- ModerateARC Teeth Whitening Pen Recalled Due to Improper Storage
FDA (Devices) · 2023-11-15
- HighFamily Dollar Pregnancy Test Recalled Due to Improper Storage Conditions
FDA (Devices) · 2023-11-15
- ModerateFixodent Denture Cream Recalled Due to Improper Storage Conditions
FDA (Devices) · 2023-11-15
- ModerateFamily Dollar marijuana test strips recalled over improper storage
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 temperature
See all →- HighPotato Salad Recalled for Improper Temperature Storage During Distribution
FDA (Food) · 2024-02-14
- ModeratePrescription drug SPIRIVA recalled for temperature storage deviation
FDA (Drugs) · 2024-01-03
- ModeratePain Reliever Caplets Recalled for Improper Storage Temperature
FDA (Drugs) · 2022-08-31
- HighMultiple Cold and Flu Medications Recalled Due to Improper Storage Conditions
FDA (Drugs) · 2022-08-31
- ModerateBlistex Lip Medex Recalled Due to Improper Storage Conditions
FDA (Drugs) · 2022-08-31