FDAClass IIIJuly 11, 2012

Imodium Multi-Symptom Relief Caplets recall

Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of…

Why was Imodium Multi-Symptom Relief Caplets recalled?

Defective Container; damaged blister units

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #CMF023, Expiration 07/13.

Product
Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of…
Recalling firm
Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.
Quantity
53,892 packages
Distribution
Nationwide
Recall date
July 11, 2012
Classification
Class III
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls