FDA recall record

Amerisource Health Services Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate recall — FDA D-1486-2016

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIclassification
D-1486-2016official record ID
Sep 14, 2016report date

Recall record at a glance

Official recordD-1486-2016
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmerisource Health Services
Report dateSep 14, 2016
Recall initiation dateAug 24, 2016
Quantity834 cartons
LocationColumbus, OH, United States

Official product description

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 10 mg 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-815-25; Blister NDC 68084-815-95

Why the product was recalled

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Distribution information

Product was distributed in the following states: Nationwide

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

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.