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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,468 in last 12 months

Showing 3134131360 of 49,976 recalls

Medical DeviceDecember 20, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Na+ Slides Recalled by Ortho-Clinical Diagnostics Due to There is a...

The Issue: There is a potential for biased results to be generated over the 10 day...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Becton Dickinson & Company

Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...

The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Recalled by GE...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Zimmer Biomet, Inc.

Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...

The Issue: Product complaints indicated that the part and lot numbers on the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Zimmer Biomet, Inc.

Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...

The Issue: Product complaints indicated that the part and lot numbers on the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Beckman Coulter Inc.

Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Bard Access Systems

Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....

The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Bard Access Systems

Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...

The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...

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

Class II — Potential Health HazardOngoing
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Bakers Corner Vanilla Instant Pudding & Pie Filling Recalled by Subco Foods...

The Issue: Subco Foods of Wisconsin was notified by their supplier that the high heat...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Best Choice Pistachio Instant Pudding & Pie Filling Recalled by Subco Foods...

The Issue: Subco Foods of Wisconsin was notified by their supplier, that the high heat...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Best Choice French Vanilla Instant Pudding & Pie Filling Recalled by Subco...

The Issue: Subco Foods of Wisconsin was notified by their supplier that the high heat...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Best Choice Lemon Instant Pudding & Pie Filling Recalled by Subco Foods of...

The Issue: Subco Foods of Wisconsin was notified by their supplier that the high heat...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 19, 2016· Apotex Inc.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: Product may not meet specifications throughout shelf life.

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2016· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM INJECTION Recalled by Fresenius Kabi USA, 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
DrugDecember 16, 2016· Aurobindo Pharma USA Inc

Recalled Item: Pantoprazole Sodium for Injection Recalled by Aurobindo Pharma USA Inc Due...

The Issue: Discoloration: Some vials were found to contain powder with a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista AMM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Parker Medical

Recalled Item: Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker...

The Issue: The product was not functioning as intended. The ventilation to the patient...

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

Class II — Potential Health HazardOngoing