73 FDA recalls mention Dextromethorphan. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Dextromethorphan.
Reason Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.
Reason Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is…
Reason Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were inadvertently overwrapped with NyQuil Liquid Cherry information as a result the…
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading…
Reason Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or…
Reason Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
Reason Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or…
Reason Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or…
Reason Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or…
Reason Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or…
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