FDA recall D-0800-2016

Pfizer Inc · Class III · drug

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

Reason for recall

Labeling: Label Mix-Up

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2016-02-10
Report date
2016-04-06
Termination date
2016-06-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Peapack, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0800-2016