Aaron Industries Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength, Cough Cold recall — FDA D-1286-2014
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.
Overview of recall records associated with Aaron Industries Inc., including dates, categories and classifications where available.
Classification mix: Class III: 7.
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.
Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is precipitating out.
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…
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…
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…
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…
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…
This page summarizes recall records in which the official source identifies Aaron Industries Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.