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Class III: unlikely to cause harmTerminated

L. Perrigo PE Daytime Cold/Flu LiqGel Recall

PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Ph…

L. Perrigo Co. · Allegan, MI

Risk level
Class III
Reported by FDA
Apr 3, 2013
Recall ID
D-216-2013
Check your lot numberHow we source this data

Summary

L. Perrigo recalled PE Daytime Cold/Flu LiqGel starting Feb 18, 2013. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-216-2013 on Apr 3, 2013. Reason: Subpotent; 12 month time point for the active ingredient Phenylephrine HCl. Status: Terminated.

Why it was recalled

Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.

Product description

PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count blister pack, Distributed By: Wal-Mat Stores Inc., Bentonville, AR, 72716

Lot numbers, UPCs & expiration codes

2 AE1549 Exp. 02/13

Where it was sold

Walmart Distribution Center in Bentonville, AR

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-216-2013
Classification
Class III
Status
Terminated
Recall initiated
Feb 18, 2013
FDA report date
Apr 3, 2013
Quantity
60,048 Blister packs
Recall type
Voluntary: Firm initiated
Recalling firm
L. Perrigo Co.

Original FDA data

Every field from FDA enforcement report D-216-2013, exactly as published.

Show all FDA fields
City
Allegan
State
MI
Status
Terminated
Country
United States
Event ID
64388
Address
515 Eastern Ave
Code information
2 AE1549 Exp. 02/13
Postal code
49010-9070
Report date
Apr 3, 2013
Product type
Drugs
Recall number
D-216-2013
Classification
Class III
Recalling firm
L. Perrigo Co.
Product quantity
60,048 Blister packs
Termination date
Sep 12, 2013
Reason for recall
Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
Voluntary / mandated
Voluntary: Firm initiated
Product description
PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count blister pack, Distributed By: Wal-Mat Stores Inc., Bentonville, AR, 72716
Distribution pattern
Walmart Distribution Center in Bentonville, AR
Recall initiation date
Feb 18, 2013
Initial firm notification
Letter
Center classification date
Mar 22, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-216-2013, published Apr 3, 2013. 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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