D-1404-2012 Class III Terminated
FDA drug recall D-1404-2012 was initiated by Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc. on May 17, 2012 and is designated Class III. Reason for recall: Defective Container; damaged blister units The recall status is terminated (terminated April 11, 2013). Affected quantity: 53,892 packages.
Recall Details
- Product Type
- Drugs
- Report Date
- July 11, 2012
- Initiation Date
- May 17, 2012
- Termination Date
- April 11, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 53,892 packages
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
Reason for Recall
Defective Container; damaged blister units
Distribution Pattern
Nationwide
Code Information
Lot #CMF023, Expiration 07/13.