Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,620 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,620 in last 12 months

Showing 35813600 of 13,363 recalls

DrugNovember 12, 2021· SterRx, LLC

Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Fentanyl Citrate Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE 4 mg per 250 mL (16 mcg per mL) in 5% Dextrose Injection...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: PHENYLepherine HCL in 0.9% Sodium Chloride Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Midazolam in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Fentanyl Citrate Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: dilTIAZem HCl 125 mg per 125 mL (1 mg per mL) in 0.7% Sodium Chloride...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2021· PAR Sterile Products LLC

Recalled Item: Buprenorphine HCl Recalled by PAR Sterile Products LLC Due to...

The Issue: Crystallization: presence of white, crystalline product agglomeration...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2021· Medline Industries Inc

Recalled Item: Hand Sanitizer Foam (ethyl alcohol) Recalled by Medline Industries Inc Due...

The Issue: Defective Container: Customer complaints for leaking bottles and dispensing...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2021· TOLMAR, Inc.

Recalled Item: Clindamycin and Benzoyl Peroxide Gel Recalled by TOLMAR, Inc. Due to...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 3, 2021· Ascend Laboratories LLC

Recalled Item: Cefixime Capsules 400 mg Recalled by Ascend Laboratories 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
DrugNovember 1, 2021· Precision Dose Inc.

Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...

The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2021· Precision Dose Inc.

Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...

The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2021· Teva Pharmaceuticals USA

Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund