Walgreens Daytime and Nighttime Cold & Flu — Class III drug recall D-0925-2017
Terminated recall by L. Perrigo Company, reported 2017-07-05, distributed in IL. Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin
| Recall number | D-0925-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | L. Perrigo Company, Allegan, MI, United States |
| Recall initiated | 2017-06-05 |
| Classified | 2017-06-28 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2017-12-07 |
| Distributed | IL |
| Quantity | 1,998 combo |
| Reason classes | labeling |
| Lot numbers | 10/18, 6MV0944 |
Product
Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by one paper sleeve, TOTAL 24 FL OZ (1.5 pt)(710 mL), OTC, Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015
Reason for recall
Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Cough Liquid.
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-0925-2017. 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.