FDA recall record

Apace KY Amantadine HCl Capsules, USP, 100 mg recall — FDA D-1035-2017

Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg

Class IIclassification
D-1035-2017official record ID
Aug 9, 2017report date

Recall record at a glance

Official recordD-1035-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmApace KY LLC
Report dateAug 9, 2017
Recall initiation dateJun 19, 2017
Quantity1,483 cartons
LocationFountain Run, KY, United States

Official product description

Amantadine HCl Capsules, USP, 100 mg, Rx Only, 50 Capsules (5x10) Unit Dose Cartons, Manufactured for: AvKARE Inc, Pulaski, TN 38478 --- NDC: 50268-0069-15

Why the product was recalled

Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg

Distribution information

KY

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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

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