Hazard
65 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 65 temperature deviation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all temperature deviation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Cardinal Healthcare is recalling Donepezil Hydrochloride 5 mg tablets (Batch 17605) distributed nationwide because they were exposed to temperatures outside labeled storage conditions, which could affect drug stability.
Cardinal Healthcare is recalling low-dose aspirin tablets nationwide due to a CGMP deviation involving improper storage temperatures. Products may have been exposed to conditions outside the manufacturer's labeled storage requirements, potentially affecting product stability.
CARDINAL HEALTHCARE is recalling Amoxicillin for Oral Suspension nationwide due to CGMP deviations. Products were exposed to temperatures outside their labeled storage conditions.
Cardinal Healthcare is recalling Citalopram 20mg tablets (batch 3131748) nationwide due to exposure to temperatures outside labeled storage conditions during manufacturing.
Cardinal Healthcare is recalling Leader Nasal Decongestant PE (Phenylephrine HCl 10 mg, 18-tablet cartons) nationwide because products were exposed to temperatures outside the labeled storage conditions. Batch P125514 is affected.
Family Dollar Stores is recalling Advil Ibuprofen 200mg caplets stored outside temperature requirements. The recall affects units distributed nationwide from July 2022 through March 2023.
Family Dollar Stores is recalling MIRALAX 8.3 OZ (SKU 902219) distributed nationwide from April 30 to June 10, 2022. The product was held outside appropriate storage temperatures, violating manufacturing standards.
Family Dollar Stores is recalling three NPX antibiotic ointment products due to improper storage temperature conditions that may affect product quality. Consumers should return or discard the products.
Witch hazel product distributed to Family Dollar Stores from April through June 2022 was stored at improper temperatures. The FDA issued a Class II recall due to manufacturing and quality control (CGMP) deviations.
Family Dollar Stores is recalling multiple eye drop products that were held outside appropriate storage temperature conditions. These products were distributed nationwide between April 30 and June 10, 2022.
Family Dollar Stores is recalling Vicks DayQuil/NyQuil Liquid combination packs (SKU 903367) distributed from April 30 to June 10, 2022, due to improper storage temperatures that may affect medication effectiveness.
Family Dollar Stores is recalling QP Sudfedrine PE Max Strength tablets nationwide due to storage temperature deviations that may have compromised product quality.
Family Dollar Stores is recalling multiple Tylenol and acetaminophen products due to CGMP deviations involving improper storage temperature conditions. Products were distributed nationwide through specific Family Dollar locations from April 30, 2022 through June 10, 2022.
Family Dollar Stores is recalling multiple allergy and sinus medications because they were held outside appropriate storage temperature conditions, which may affect their safety and efficacy.
Family Dollar Stores recalled two antifungal products due to storage temperature deviations. The products may have been compromised in effectiveness due to failure to maintain proper storage conditions.
Family Dollar Stores recalled Swan Povidone 4 FL OZ due to storage temperature deviations that may affect product quality. Products distributed nationwide from April to June 2022 should not be used.
Family Dollar Stores is recalling Excedrin Migraine Caplets (24 CT) due to improper storage temperature conditions that may affect product quality. Affected products were distributed nationwide between April 30 and June 10, 2022.
Family Dollar Stores is recalling specific CLARITIN allergy products (liquids and tablets) distributed from April through June 2022 due to improper storage temperature conditions that may affect product quality.
Family Dollar Stores recalled MIDOL COMPLETE, QP MENSTRUAL RELIEF, and QP PMS FORMULA caplets distributed April–June 2022 due to CGMP deviations from improper storage temperature.
Family Dollar is recalling Stye Eye Ointment 0.125 oz due to manufacturing deviations. The product was held outside appropriate storage temperature conditions.
Family Dollar Stores is recalling Preferred Urinary Pain Relief Max Strength due to CGMP violations involving improper storage temperature. Product was distributed nationwide April 30 through June 10, 2022.
Family Dollar Stores is recalling DRX Fiber Capsules (100 CT) distributed nationwide April 30–June 10, 2022, due to improper storage temperature conditions that violate good manufacturing practice requirements.
Zarbee's Naturals baby cough syrup has been recalled due to storage temperature deviations at Family Dollar stores between April and June 2022.
Family Dollar Stores is recalling Zarbee's Natural Children's Cough + Mucus syrup distributed April through June 2022 due to CGMP violations involving improper storage temperature conditions that may compromise product quality.
Family Dollar sleep aid products were distributed outside proper temperature storage conditions. Consumers should stop using affected products and consult their healthcare provider if concerned.