D-0925-2017 Class III Terminated
FDA drug recall D-0925-2017 was initiated by L. Perrigo Company on Jun 5, 2017 and is designated Class III. 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… The recall status is terminated (terminated Dec 7, 2017). Affected quantity: 1,998 combo packs.
Recall Details
- Product Type
- Drugs
- Report Date
- Jul 5, 2017
- Initiation Date
- Jun 5, 2017
- Termination Date
- Dec 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,998 combo packs
Product Description
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.
Distribution Pattern
IL
Code Information
Lot #: 6MV0944, Exp 10/18
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0925-2017
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026