FDA Drug recall D-0800-2016
Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz
- FDA Drug
- Class III
- terminated
- Published 2016-04-06
On 2016-04-06 the FDA classified a Class III recall of Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz by Pfizer, citing labeling: Label Mix-Up.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0800-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-02-10 |
| Published | 2016-04-06 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Pfizer |
| Distribution | US |
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
Labeling: Label Mix-Up
Identifiers
| code_info | Lot #: R29364; Exp. 10/17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0800-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.