PE Daytime Cold/Flu LiqGel recall: Subpotent
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
Why was PE Daytime Cold/Flu LiqGel recalled?
Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
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?
2 AE1549 Exp. 02/13
- Product
- 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
- Recalling firm
- L. Perrigo Co.
- Quantity
- 60,048 Blister packs
- Distribution
- Walmart Distribution Center in Bentonville, AR
- Recall date
- April 3, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)