Drug recall D-188-2013
Product
Wal-Mart Equate Tussin CF Adult Maximum Strength, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (235 mL) (NDC 49035-229-08; UPC Code: 6-81131-03884-30), Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72712.
Reason for recall
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.
Lots and codes
Lot# 81198, 82183, 80797; FP-44-081-03884,
Recall details
- Recalling firm
- Aaron Industries Inc, Lynwood, CA
- Quantity
- 43,464 bottles (3,622 cases)
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 18, 2013
- Terminated
- November 1, 2013
Related products
- NDC 49035-229 Acne Treatment · Benzoyl Peroxide 100 mg/g · Walmart Inc.