Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,759 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,759 in last 12 months

Showing 84218440 of 13,449 recalls

DrugDecember 22, 2016· Aurobindo Pharma USA Inc

Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...

The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Roxane Laboratories, Inc.

Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2016· Accord Healthcare, Inc.

Recalled Item: Lisinopril tablets Recalled by Accord Healthcare, Inc. Due to Failed...

The Issue: Failed tablet/capsule specification: missing break line on the 5mg tablet.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2016· Apotex Inc.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: Product may not meet specifications throughout shelf life.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2016· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2016· Aurobindo Pharma USA Inc

Recalled Item: Pantoprazole Sodium for Injection Recalled by Aurobindo Pharma USA Inc Due...

The Issue: Discoloration: Some vials were found to contain powder with a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 14, 2016· Roxane Laboratories, Inc.

Recalled Item: Azelastine Hydrochloride Nasal Solution (Nasal Spray) Recalled by Roxane...

The Issue: Defective Delivery System: out of specification result for droplet size...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 13, 2016· Pacific Medical Solutions

Recalled Item: Nano PNC Water Recalled by Pacific Medical Solutions Due to Marketed without...

The Issue: Marketed without an Approved NDA/ANDA and non-sterility: NANO PNC Water by...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 13, 2016· Sandoz Inc

Recalled Item: Donepezil Hydrochloride Tablets Recalled by Sandoz Inc Due to Subpotent...

The Issue: Subpotent Drug: out of specification results for assay test.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Virt-Select Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Extra-Virt Plus DHA Prenatal/Postnatal Softgel Recalled by VIRTUS...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· Amneal Pharmaceuticals LLC

Recalled Item: Rabeprazole Sodium Delayed Release Tablets Recalled by Amneal...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: VirtPrex Prenatal/Postnatal Tablets Recalled by VIRTUS PHARMACEUTICALS OPCO...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Virt-Advance Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund