FDAClass IIIApril 6, 2016

Adult Robitussin PEAK COLD Cough & Chest Congestion DM recall: Labeling Error

Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ 07940, NDC 0031-8736-18

Why was Adult Robitussin PEAK COLD Cough & Chest Congestion DM recalled?

Labeling: Label Mix-Up

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: R29364; Exp. 10/17

Product
Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ 07940, NDC 0031-8736-18
Recalling firm
Pfizer Inc
Quantity
63,636 plastic bottles
Distribution
Nationwide
Recall date
April 6, 2016
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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