Pfizer Inc recalls Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ…
- Recall date
- February 10, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0800-2016
- FDA classification
- Class III
- Brand / firm
- Pfizer Inc
- Sold / distributed
- Nationwide
Why it was recalled
Labeling: Label Mix-Up
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ 07940, NDC 0031-8736-18
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