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. 2,664 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,664 in last 12 months

Showing 41214140 of 13,376 recalls

DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Toposar (etoposide injection USP) Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pantoprazole Sodium for Injection 40mg/vial For I.V. infusion only...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Apotex Corp.

Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...

The Issue: Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 2, 2021· Apotex Corp.

Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...

The Issue: Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 1, 2021· Kimberly-Clark Corporation

Recalled Item: Scott¿ Moisturizing Foam Hand Sanitizer Recalled by Kimberly-Clark...

The Issue: Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2021· Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2021· Accord Healthcare, Inc.

Recalled Item: Glycopyrrolate Injection Recalled by Accord Healthcare, Inc. Due to...

The Issue: Labeling; Label Mix-up; correctly labeled 2 mL vials were packaged into...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2021· Meitheal Pharmaceuticals Inc

Recalled Item: Cisatracurium Besylate Injection Recalled by Meitheal Pharmaceuticals Inc...

The Issue: Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 27, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...

The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg...

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

Class I — Serious Health HazardOngoing
Refund