FDA recall record

L. Perrigo Co PE Daytime Cold/Flu LiqGel, Multi Symptom Relief recall — FDA D-216-2013

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

Class IIIclassification
D-216-2013official record ID
Apr 3, 2013report date

Recall record at a glance

Official recordD-216-2013
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmL. Perrigo Co.
Report dateApr 3, 2013
Recall initiation dateFeb 18, 2013
Quantity60,048 Blister packs
LocationAllegan, MI, United States

Official 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

Why the product was recalled

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

Distribution information

Walmart Distribution Center in Bentonville, AR

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.