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Class III: unlikely to cause harmTerminated

L. Perrigo Walgreens Daytime and Nighttime Cold & Flu Recall

Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL…

L. Perrigo Company · Allegan, MI

Risk level
Class III
Reported by FDA
Jul 5, 2017
Recall ID
D-0925-2017
Check your lot numberHow we source this data

Summary

L. Perrigo recalled Walgreens Daytime and Nighttime Cold & Flu starting Jun 5, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0925-2017 on Jul 5, 2017. Reason: 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. Status: Terminated.

Why it was recalled

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.

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

Lot numbers, UPCs & expiration codes

Lot #: 6MV0944, Exp 10/18

Where it was sold

IL

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0925-2017
Classification
Class III
Status
Terminated
Recall initiated
Jun 5, 2017
FDA report date
Jul 5, 2017
Quantity
1,998 combo packs
Recall type
Voluntary: Firm initiated
Recalling firm
L. Perrigo Company

Original FDA data

Every field from FDA enforcement report D-0925-2017, exactly as published.

Show all FDA fields
City
Allegan
State
MI
Status
Terminated
Country
United States
Event ID
77450
Address
515 Eastern Ave
Code information
Lot #: 6MV0944, Exp 10/18
Postal code
49010-9070
Report date
Jul 5, 2017
Product type
Drugs
Recall number
D-0925-2017
Classification
Class III
Recalling firm
L. Perrigo Company
Product quantity
1,998 combo packs
Termination date
Dec 7, 2017
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.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
IL
Recall initiation date
Jun 5, 2017
Initial firm notification
Letter
Center classification date
Jun 28, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0925-2017, published Jul 5, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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