Aaron Industries Inc
Complete recall history across all FDA and CPSC categories — 7 total recalls
Aaron Industries Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Drug Recalls (7)
FDA drug safety enforcement actions by Aaron Industries Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 11, 2014 | Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength, Cough Cold, Dex... | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ... | Class III |
| Feb 4, 2014 | Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan ... | Presence of Precipitate: Recall is due to complaints of a white substance, co... | Class III |
| Apr 4, 2013 | Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextrom... | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ... | Class III |
| Jan 18, 2013 | Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi... | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ... | Class III |
| Jan 18, 2013 | Wal-Mart Equate Tussin CF Adult Maximum Strength, Multi-Symptom Cold, (dextro... | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ... | Class III |
| Jan 18, 2013 | Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextro... | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ... | Class III |
| Jan 18, 2013 | Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorp... | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ... | Class III |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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