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American Health Packaging Recalls
59 recalls on record · August 22, 2012 to May 25, 2022 · Drugs
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 21, 2018DrugsFDA
AMERICAN HEALTH PACKAGING recalls Aripiprazole Tablets, USP, 10 mg, 100 Tablets (10 x 10) unit dose blisters [NDC60687-179-11; UPC (01) 003 60687 179 11 7
Hazard: CGMP Deviations: lot made with active pharmaceutical ingredient that did not meet all its intended specifications.
July 22, 2015DrugsFDA
American Health Packaging recalls Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed b
Hazard: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
July 15, 2015DrugsFDA
American Health Packaging recalls Zonisamide capsules, USP 100mg packaged in 10-count blisters (NDC 68084-008-11); 5 blister packs per carton (NDC 68084-0
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Lisinopril tablets, USP 40mg packaged in 10-count blisters (NDC 68084-064-11); 10 blister packs per carton (NDC 68084-06
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Lisinopril tablets, USP 20mg packaged in 10-count blisters (NDC 68084-062-11); 10 blister packs per carton (NDC 68084-06
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Lisinopril tablets, USP 10mg packaged in 10-count blisters (NDC 68084-061-11); 10 blister packs per carton (NDC 68084-06
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Lisinopril tablets, USP 5mg packaged in 10-count blisters (NDC 68084-060-11); 10 blister packs per carton (NDC 68084-060
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Famotidine tablets, USP 20mg, packaged in 10-count blisters (NDC 68084-172-11); 10 blister packs per carton (NDC 68084-1
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Clarithromycin tablets, USP 500mg, packaged in 10-count blisters (NDC 68084-437-11); 5 blister packs per carton (NDC 680
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Azithromycin tablets, USP 250mg, packaged in 10-count blisters (NDC 68084-278-11); 10 blister packs per carton (NDC 6808
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Azithromycin tablets, USP 600mg, packaged in 10-count blisters (NDC 68084-464-11); 3 blister packs per carton (NDC 68084
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Azithromycin tablets, USP 500mg, packaged in 10-count blisters (NDC 68084-279-11); 3 blister packs per carton (NDC 68084
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Amlodipine besylate tablets, USP 10 mg, packaged in 10-count blisters (NDC 68084-506-11); 10 blister packs per carton (N
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Amlodipine besylate tablets, USP 5mg, packaged in 10-count blisters (NDC 68084-505-11); 10 blister packs per carton (NDC
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
July 15, 2015DrugsFDA
American Health Packaging recalls Amlodipine besylate tablets, USP 2.5mg, packaged in 10-count blisters (NDC 68084-498-11); 10 blister packs per carton (N
Hazard: CGMP Deviations: Firm did not adequately investigate customer complaints.
June 24, 2015DrugsFDA
American Health Packaging recalls Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American
Hazard: Failed dissolution specifications
April 8, 2015DrugsFDA
American Health Packaging recalls Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Co
Hazard: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
December 24, 2014DrugsFDA
American Health Packaging recalls Mercaptopurine Tablets, USP, 50 mg, 30 Tablets (3 x 10) unit dose blisters per carton, Rx only, Manufactured by Promethe
Hazard: Failed USP Dissolution Test Requirements: This sub-recall is in response to Prometheus Laboratories Inc. recall for Mercaptopurine USP 50mg because the lot does not meet the specification for dissolution.
October 29, 2014DrugsFDA
American Health Packaging recalls MethylPREDNISolone Tablets, USP, 4 mg, 100 unit dose blisters, Packaged and Distributed by: American Health Packaging, C
Hazard: Subpotent; 6 month stability time point
September 24, 2014DrugsFDA
American Health Packaging recalls Oxcarbazepine Tablets, 300 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health P
Hazard: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544.
September 24, 2014DrugsFDA
American Health Packaging recalls Ibuprofen Tablets, USP, 600 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health
Hazard: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544
April 9, 2014DrugsFDA
American Health Packaging recalls HydrOXYzine HCl Tablets, USP 50 mg, 100 Tablet Blister, Rx only Mfd by: KVK-TECH, INC. Newtown, PA 18940, NDC 68084-255
Hazard: Good Manufacturing Practices Deviations: The product has an active pharmaceutical ingredient from an unapproved source.
April 9, 2014DrugsFDA
American Health Packaging recalls HydrOXYzine HCl Tablets, USP 25 mg, 100 Tablet Blister, Rx only Mfd by: KVK-TECH, INC. Newtown, PA 18940, NDC 68084-254
Hazard: Good Manufacturing Practices Deviations: The product has an active pharmaceutical ingredient from an unapproved source.
December 11, 2013DrugsFDA
American Health Packaging recalls Valacyclovir HCl Tablets, 500 mg, 100 tablets (10x10) blister cards, Rx only, Packaged and Distributed by: American Heal
Hazard: Subpotent
August 21, 2013DrugsFDA
American Health Packaging recalls buPROPion Hydrochloride Extended Release Tablets, USP 100 mg, 100 count carton, 10 blister cards of 10 individually blis
Hazard: Failed Stability Specifications; out of specification results at the 9 month stability time point for color, dissolution and related compounds.
August 14, 2013DrugsFDA
American Health Packaging recalls Zolpidem Tartrate Tablets 5 mg, 10 tablets per blister, 10 blisters per carton, 100 cartons per box, Rx Only, Manufactur
Hazard: Unit Dose Mispackaging: This recall event is due to a random undetected packaging issue which could increase the potential for a small number of individual unit dose blisters to be packed with more than one tablet.
July 24, 2013DrugsFDA
American Health Packaging recalls QUETIAPINE Fumarate Tablets 25mg 100 Tablets (10x10) Blister card, Rx, Packaged and Distributed by: American Health Pac
Hazard: Failed Dissolution Test Requirements: During analysis of long term stability studies at 3 months time point, an OOS was reported for Quetiapine Fumarate Tablets, 25 mg.
September 5, 2012DrugsFDA
American Health Packaging recalls Mercaptopurine Tablets, USP, 50 mg, 30 Tablets (3 x 10) unit dose blisters per carton, Rx only, Packaged by American Hea
Hazard: Failed USP Dissolution Test Requirements: This sub-recall is in response to Prometheus Laboratories Inc. recall for Mercaptopurine USP 50mg because the lot does not meet the specification for dissolution.
August 22, 2012DrugsFDA
American Health Packaging recalls Topiramate Tablets, 50 mg, 30-count (3 x 10) unit-dose blisters per carton, Rx only, Mfd by: Cadila Healthcare Ltd., Ahm
Hazard: Labeling: Label Mix-Up: A typographical error in the product form on the carton label incorrectly lists the configuration as 30 "Capsules" (3 x 10) rather than "Tablets".