Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 75076

10 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 24, 2016
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Amerisource Health Services

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

10 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-874-25; Blister NDC 68084-874-95

D-1481-2016
Recall number
D-1481-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
221 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 163220, exp. 10/31/17 and lot 164194, exp. 11/20/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 2 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 10 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-936-25; Blister NDC 68084-936-95

D-1482-2016
Recall number
D-1482-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
2,276 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 150130, exp. 10/31/16 and lot 161296, exp. 8/31/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 3 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 15 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 60687-133-25; Blister NDC 60687-133-95

D-1483-2016
Recall number
D-1483-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
1,416 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 150950, exp. 3/31/17 and lot 154813, exp. 5/31/2017

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 4 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-943-25; Blister NDC 68084-943-95

D-1484-2016
Recall number
D-1484-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
867 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 162276, exp. 9/30/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 5 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 60687-154-25; Blister NDC 60687-154-95

D-1485-2016
Recall number
D-1485-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
156 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 162278, exp. 10/31/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 6 of 10

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

D-1486-2016
Recall number
D-1486-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
834 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 152254, exp. 12/31/16, lot 152324, exp. 3/31/17, lot 154833, exp. 5/31/17, lot 162406, exp. 12/31/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 7 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 15 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-898-32; Blister NDC 68084-898-33

D-1487-2016
Recall number
D-1487-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
126 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 162489, exp. 9/30/17 and lot 162910, exp. 10/31/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 8 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-832-25; Blister NDC 68084-832-95

D-1488-2016
Recall number
D-1488-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
666 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 152325, exp. 12/31/16, lot 154834, exp. 5/31/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 9 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 25 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-909-32; Blister NDC 68084-909-33

D-1489-2016
Recall number
D-1489-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
115 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 162490, exp. 9/30/17

Distribution pattern

Product was distributed in the following states: Nationwide

drug · product 10 of 10

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-887-32; Blister NDC 68084-887-33

D-1490-2016
Recall number
D-1490-2016
Initiated
August 24, 2016
Classification
Class II
Status
Terminated
Quantity
761 cartons

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Mispackaging

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 152418, exp. 12/31/16, lot 153544, exp. 3/31/17, lot 154835, exp. 5/31/17

Distribution pattern

Product was distributed in the following states: Nationwide

Field note

Send feedback

We'll only use this to respond to your feedback.