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. 2,654 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,654 in last 12 months

Showing 57415760 of 13,376 recalls

DrugJune 7, 2019· Akorn Inc

Recalled Item: Myorisan (isotretinoin capsules Recalled by Akorn Inc Due to Labeling: Label...

The Issue: Labeling: Label mix-up: Product secondary carton erroneously states 40mg...

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

Class III — Low RiskOngoing
Refund
DrugJune 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 100 mg TABLET BULK 90 count bottles Recalled by Teva...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg/ Recalled by...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due to...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine HCL Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Recalled by Sun...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due to...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Estradiol Vaginal Inserts USP 10 mcg Recalled by Glenmark Pharmaceuticals...

The Issue: Defective Delivery System: Estradiol Vaginal Inserts USP plunger is not...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium) Recalled by...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Geri-Tussin DM Recalled by Geritrex, LLC Due to cGMP Deviations:...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Ritussin DM Double Strength Recalled by Geritrex, LLC Due to cGMP...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Chiesi USA, Inc.

Recalled Item: ZYFLO CR (zileuton) extended-release tablets Recalled by Chiesi USA, Inc....

The Issue: Failed Dissolution Specifications: Out of specification result for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Diocto Liquid Docusate Sodium Stool Softener Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Ritussin DM Children & Adults Recalled by Geritrex, LLC Due to cGMP...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Chiesi USA, Inc.

Recalled Item: Zileuton Extended-Release Tablets Recalled by Chiesi USA, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Out of specification result for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Iron Supplement Elixir Ferrous Sulfate Recalled by Geritrex, LLC...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund