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Class III: unlikely to cause harmTerminated

Mcneil Consumer Healthcare, Div Of Mcneil-ppc Imodium Multi-Symptom Relief Caplets Recall

Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count…

Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc. · Fort Washington, PA

Risk level
Class III
Reported by FDA
Jul 11, 2012
Recall ID
D-1404-2012
Check your lot numberHow we source this data

Summary

Mcneil Consumer Healthcare, Div Of Mcneil-ppc recalled Imodium Multi-Symptom Relief Caplets starting May 17, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1404-2012 on Jul 11, 2012. Reason: Defective Container; damaged blister units. Status: Terminated.

Why it was recalled

Defective Container; damaged blister units

Product description

Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of McNeil-PPC Inc., Fort Washington, PA

Lot numbers, UPCs & expiration codes

Lot #CMF023, Expiration 07/13.

Where it was sold

Nationwide

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-1404-2012
Classification
Class III
Status
Terminated
Recall initiated
May 17, 2012
FDA report date
Jul 11, 2012
Quantity
53,892 packages
Recall type
Voluntary: Firm initiated
Recalling firm
Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.

Original FDA data

Every field from FDA enforcement report D-1404-2012, exactly as published.

Show all FDA fields
City
Fort Washington
State
PA
Status
Terminated
Country
United States
Event ID
61872
Address
7050 Camp Hill Rd
Code information
Lot #CMF023, Expiration 07/13.
Postal code
19034-2210
Report date
Jul 11, 2012
Product type
Drugs
Recall number
D-1404-2012
Classification
Class III
Recalling firm
Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.
Product quantity
53,892 packages
Termination date
Apr 11, 2013
Reason for recall
Defective Container; damaged blister units
Voluntary / mandated
Voluntary: Firm initiated
Product description
Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of McNeil-PPC Inc., Fort Washington, PA
Distribution pattern
Nationwide
Recall initiation date
May 17, 2012
Initial firm notification
Letter
Center classification date
Jul 2, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1404-2012, published Jul 11, 2012. 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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