Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,642 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,642 in last 12 months

Showing 83618380 of 13,376 recalls

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· 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 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: 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
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: 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 7, 2016· Novum Pharma, LLC

Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate Recalled by Novum...

The Issue: Subpotent Drug: Out of specification result for pramoxine hydrochloride

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

Class III — Low RiskOngoing
Refund
DrugDecember 2, 2016· Shire PLC

Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...

The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...

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

Class III — Low RiskOngoing
Refund
DrugDecember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Risedronate Sodium Delayed-release Tablets Recalled by Teva Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 22, 2016· Pfizer Inc.

Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....

The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...

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

Class III — Low RiskOngoing
Refund
DrugNovember 22, 2016· Les Emballages Knowlton Inc.

Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...

The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.

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

Class III — Low RiskOngoing
Refund