Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz — Class III drug recall D-0800-2016
Terminated recall by Pfizer Inc, reported 2016-04-06, distributed nationwide. Labeling: Label Mix-Up
| Recall number | D-0800-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pfizer Inc, Peapack, NJ, United States |
| Recall initiated | 2016-02-10 |
| Classified | 2016-03-31 |
| Reported by FDA | 2016-04-06 |
| Terminated | 2016-06-22 |
| Distributed | Nationwide (US) |
| Quantity | 63,636 plastic |
| Reason classes | labeling |
| NDC | 00031-8736-18 |
| Lot numbers | 10/17, R29364 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0800-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.