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. 2,598 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,598 in last 12 months

Showing 74617480 of 50,117 recalls

DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 31, 2023· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Positioner Arm may not tighten or lock during normal use.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· BioReference Health, LLC

Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...

The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· Folsom Metal Products, Inc.

Recalled Item: Small DKS Disposable Kerrison System Recalled by Folsom Metal Products, Inc....

The Issue: Units were not intended for commercial distribution and inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· Folsom Metal Products, Inc.

Recalled Item: DKS Disposable Kerrison System Recalled by Folsom Metal Products, Inc. Due...

The Issue: Units were not intended for commercial distribution and inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· KENT IMAGING, INC.

Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...

The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...

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

Class II — Potential Health HazardOngoing
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Lisinopril Tablets USP 20 mg Recalled by NCS Healthcare of Kentucky Inc Due...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Buspirone Hydrochloride Tabs USP 10 mg Recalled by NCS Healthcare of...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Extended Phenytoin Sodium Capsules Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2023· VistaPharm LLC

Recalled Item: Mycophenolate Mofetil for Oral Suspension Recalled by VistaPharm LLC Due to...

The Issue: Defective Container: The adaptor does not fit into the neck of the bottle...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· PHASE SCIENTIFIC INTERNATIONAL LIMITED

Recalled Item: INDICAID COVID-19 Rapid Antigen At-Home Test Recalled by PHASE SCIENTIFIC...

The Issue: COVID-19 rapid antigen at home tests were released with an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Becton, Dickinson and Company, BD Biosciences

Recalled Item: CD11b APC: ASR Recalled by Becton, Dickinson and Company, BD Biosciences Due...

The Issue: In vitro diagnostics product that impacts the quality of cell staining can...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Riverpoint Medical, LLC

Recalled Item: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) Recalled by...

The Issue: Use of a 1.4 drill in hard bone conditions caused increased insertion forces...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· GRAPHENANO DENTAL SL

Recalled Item: GRAPHENANO DENTAL G-CAM Recalled by GRAPHENANO DENTAL SL Due to Machining...

The Issue: Machining error on cams renders the device unusable.

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

Class II — Potential Health HazardOngoing