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. 2,420 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,420 in last 12 months

Showing 3142131440 of 50,117 recalls

Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Bio mCT-S(40) 3R->4R Upgrade Recalled by Siemens Medical Solutions USA Inc....

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· US Endoscopy Group Inc

Recalled Item: Roth Net Polyp Retrieval Recalled by US Endoscopy Group Inc Due to The firm...

The Issue: The firm was notified that the expiration date on the outer carton is...

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

Class III — Low RiskOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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· 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 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· 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· 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
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: 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· 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: 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· 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
FoodDecember 10, 2016· Shearers Foods, Llc

Recalled Item: SPICY NACHO CHEESE TORTILLA CHIPS: Essential Everyday 10 oz bag Recalled by...

The Issue: The firm is recalling various snack products because they used ingredients...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 10, 2016· Shearers Foods, Llc

Recalled Item: Larry The Cable Guy Biscuits & Gravy Thin Potato Chips Recalled by Shearers...

The Issue: The firm is recalling various snack products because they used ingredients...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 10, 2016· Shearers Foods, Llc

Recalled Item: Larry The Cable Guy Jalapeno' Popper Thin Potato Chips 3 Recalled by...

The Issue: The firm is recalling various snack products because they used ingredients...

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

Class I — Serious Health HazardOngoing
Refund