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