Safety Alerts & Recalls

What does this mean?

This recall for Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle from Pfizer Inc was issued at a warehouse and retail level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you take Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle and are concerned, you should speak to your doctor or return the product to the store where you purchased it.

Pfizer Inc Recalls Single Lot of Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle

Pfizer Inc has recalled a single lot of Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle. Lot number R29364 is being recalled because of a label mix up.

Adult Robitussin PEAK COLD Cough & Chest Congestion DM contains the active ingredient dextromethorphan and guaifenesin and is commonly used in the treatment of cough and congestion. Dextromethorphan and guaifenesin is also sold under other brand names. This recall alert only applies to the single lot of Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle. No other dextromethorphan and guaifenesin products were involved in this recall.

To search and view the FDA notice about this recall, please visit: more information here

Source: FDA
Publication Date: 2016-07-06
Last Updated: 2016-07-06

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