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. 992 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
992 in last 12 months

Showing 31401–31420 of 49,976 recalls

FoodDecember 13, 2016· Williams-Sonoma

Recalled Item: Williams-Sonoma Meyer Lemon Poppy Quick bread mix Recalled by...

The Issue: Williams Sonoma was notified by their contract manufacturer that high heat...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 13, 2016· Ron's Home Style Foods, Inc.

Recalled Item: Texas Kitchen Salads Tropical Fruit Supreme KEEP Nutrition Facts Recalled by...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2016· Threshold Enterprises Ltd

Recalled Item: Source Naturals Dietary Supplement Vitamin D-3 Recalled by Threshold...

The Issue: Testing of Vitamin D-3 as a result of a consumer complaint found specific...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Extra-Virt Plus DHA Prenatal/Postnatal Softgel Recalled by VIRTUS...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: VirtPrex Prenatal/Postnatal Tablets Recalled by VIRTUS PHARMACEUTICALS OPCO...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Virt-Advance Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Virt-Select Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS...

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2016· Amneal Pharmaceuticals LLC

Recalled Item: Rabeprazole Sodium Delayed Release Tablets Recalled by Amneal...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...

The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...

The Issue: Olympus has received complaints regarding the breakage of the endoscope's...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Pentax of America Inc

Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...

The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Great Basin Scientific, Inc.

Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...

The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Medtronic Navigation, Inc.

Recalled Item: AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· MEDLINE IND

Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...

The Issue: Product was not sterilized. Product was shipped to distribution centers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Bard Access Systems

Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System Recalled...

The Issue: Merge received reports of Merge Eye Station being unable to capture images...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Bard Access Systems

Recalled Item: StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged...

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

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

Class II — Potential Health HazardOngoing
FoodDecember 9, 2016· Houdini Inc.

Recalled Item: Houdini Fabric gift basket Recalled by Houdini Inc. Due to Potential...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 9, 2016· Houdini Inc.

Recalled Item: Alfasi Chardonnay Kosher Selection Basket #847 Recalled by Houdini Inc. Due...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 9, 2016· Houdini Inc.

Recalled Item: The Classic Basket #6013 Recalled by Houdini Inc. Due to Potential...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund