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. 2,681 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,681 in last 12 months

Showing 11811200 of 13,376 recalls

DrugFebruary 9, 2024· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by The Harvard Drug Group LLC dba...

The Issue: an out of specification result obtained during routine stability testing for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Mallinckrodt Hospital Products Inc.

Recalled Item: Acthar Gel (repository corticotropin injection) 400 USP units/5mL (80 USP...

The Issue: cGMP deviations: Temperature excursion due to shipping delay from...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Mallinckrodt Hospital Products Inc.

Recalled Item: Terlivaz (terlipressin for injection) Recalled by Mallinckrodt Hospital...

The Issue: cGMP deviations: Temperature excursion due to shipping delay from...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: Arize Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: SCHWINNNG Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: Sustain Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 5, 2024· Super Chill Products

Recalled Item: Neptune's Fix Recalled by Super Chill Products Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 5, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Mesalamine Extended-Release Capsules Recalled by SUN PHARMACEUTICAL...

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

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2024· Bausch Health Companies, Inc.

Recalled Item: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1 Recalled by...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 1, 2024· Integrity Products

Recalled Item: RAM IT Recalled by Integrity Products Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Integrity Products

Recalled Item: To the Moon Capsules Recalled by Integrity Products Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Recalled Item: TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid Recalled by...

The Issue: Chemical Contamination; presence of benzene.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· NATCO Pharma Limited

Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...

The Issue: CGMP Deviations: Inadequate induction sealing on bottles, capsules were...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 1, 2024· Amerisource Health Services LLC

Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Amerisource Health Services...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: Equate Lubricant Eye Ointment (Mineral Oil 42.5% Recalled by Brassica Pharma...

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
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient Recalled by...

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
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: Lubricant PM Ointment (Mineral Oil 42.5% and White Petrolatum 57.3%)...

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
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9% Recalled by Brassica...

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
DrugJanuary 25, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35 Recalled by...

The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 25, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic...

The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...

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

Class III — Low RiskOngoing
Refund