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

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 w…

Recall #: D-0925-2017
Affected scope: 1,998 combo packs
Initiated: June 5, 2017

Compiled from official public sources by the publisher. · Updated September 2026

Verify with FDA Drug →

View my saved recalls

L. Perrigo Company recalled Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ… - a low-severity action.

Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ… was recalled by L. Perrigo Company in July 5, 2017. Reason: Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twi…. Check the official notice for the remedy. Verify recall #D-0925-2017 with the FDA Drug before acting.

The recall

L. Perrigo Company issued this low-severity FDA Drug recall-Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twi….

Low
severity level: Class III
classification: July 5, 2017
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0925-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

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.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	D-0925-2017
Date reported	July 5, 2017
Date initiated	June 5, 2017
Recalling firm	L. Perrigo Company
Firm location	Allegan, MI
Affected scope	1,998 combo packs
Distribution	IL

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (D-0925-2017) and product description against the item you own. Search the archive
Confirm the current status with FDA Drug before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on July 5, 2017. Severity: Low. Recall number: D-0925-2017.

Where was the recalled product distributed? ▼

Distribution: IL.

Should I stop using a recalled medication or medical device? ▼

Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Low), closest by report date among other firms and states.

Minivelle (estradiol Transdermal System) … 2017-07-05 Gaviscon (Alumina & Magnesium Trisilicate… 2017-07-05 BuPROPion HCL Tablets, USP, 75 mg, packag… 2017-07-05 DIASTAT(R) ANA (anti-Nuclear antibody) EU… 2017-07-05

Similar Drugs & Medications · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Progesterone Injection in Olive Oil With … 2017-07-05 Blephamide (sulfacetamide sodium and pred… 2017-07-05 Ropivacaine HCl 0.2% 400 mL Total Volume … 2017-07-12 Ropivacaine HCl 0.2% 500 mL Total Volume … 2017-07-12

Compare this recall with Kian Pee Wan Capsules, 30-count bottles → · All Drugs & Medications recalls

This recall: FDA Drug, reported July 5, 2017. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026