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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,566 in last 12 months

Showing 1844118460 of 49,976 recalls

Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2020· UNICHEM PHARMACEUTICALS USA INC

Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...

The Issue: Failed Impurities/Degradation Specifications: potential migration of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 26, 2020· Radiometer Medical ApS

Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...

The Issue: Potential risk of patient mix-up on analyzers due to software issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2020· Radiometer Medical ApS

Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...

The Issue: Potential risk of patient mix-up on analyzers due to software issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· The Harvard Drug Group

Recalled Item: Doxycycline Hyclate Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specification: The dissolution test at the 24 month time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 22, 2020· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F Recalled...

The Issue: Due to adverse events received by the firm for left atrial perforations and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...

The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing