Aaron Industries Inc

FDA recalling firm · 4 enforcement events · 7 product records · 2013–2014 · CA

Aaron Industries Inc has 4 FDA enforcement events on this register (7 product records) between 2013 and 2014: 4 drug; the busiest year was 2013 with 2.

0% of its events are Class I; the most common class is Class III (4). 0 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
11 Apr 2014	Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength, Cough Cold, Dextromethorphan HBr, USP, 10 mg (Cough Suppressant) , Guaifenesin, USP, 200 mg (Expectorant), 4, 8 fl oz bottles , OTC only, labeled as A) CareOne 8 fl oz bottle, Distributed by American Sales Company, Lancaster, NY 14086, UPC 341520339677, B)…	Drug	Class III	1	Terminated
4 Feb 2014	Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCl 5 mg) per 5 mL, 8 FL OZ (237 mL) bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-229-08, UPC 6 81131 03884 3.	Drug	Class III	1	Terminated
4 Apr 2013	Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl 5 mg), 4 oz. package size, Distributed by: Rite Aid, Camp Hill, PA --- UPC Code: 0 11822 57307 8.	Drug	Class III	1	Terminated
18 Jan 2013	Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (237 mL) bottles, Distributed by: Walgreen Co, Deerfield, IL 60015 ---- NDC 0363-0229-08	Drug	Class III	4	Terminated

By type and class

Drug4

Class III4

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Aaron Industries Inc by year initiated.

Questions and answers

How many FDA recalls has Aaron Industries Inc had?

4 enforcement events (7 product records) on this register, 2013–2014: 4 drug.

Are any Aaron Industries Inc recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Aaron Industries Inc recalls?

4 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.