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. 2,610 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,610 in last 12 months

Showing 53615380 of 50,117 recalls

Medical DeviceJune 11, 2024· Medical Action Industries, Inc. 306

Recalled Item: Foam Protective Pouches Recalled by Medical Action Industries, Inc. 306 Due...

The Issue: The protective pouches were identified to have been improperly labeled with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Pneumonia Panel plus Recalled by BioFire Diagnostics, LLC...

The Issue: Pneumonia panels have an increased risk of control failures due to an issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Pneumonia Panel Recalled by BioFire Diagnostics, LLC Due...

The Issue: Pneumonia panels have an increased risk of control failures due to an issue...

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

Class II — Potential Health HazardOngoing
DrugJune 10, 2024· Brands International Corporation

Recalled Item: Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone) Recalled by Brands...

The Issue: Microbial Contamination of Non-Sterile Products: confirmed presence of mold...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2024· Rygel Advanced Machines d/b/a Omtech Laser

Recalled Item: OMTech Desktop Laser Engraver Recalled by Rygel Advanced Machines d/b/a...

The Issue: Lack of redundant interlocks, missing required labels and certification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2024· Randox Laboratories Ltd.

Recalled Item: RX Series CYSC- Cystatin C Reagent -Intended for in vitro Recalled by Randox...

The Issue: Cystatin C Reagent marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Beckman Coulter Mishima K.K.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...

The Issue: There are two software bug issues with the analyzer. Issue 1: When a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 3.0T. 16-element receive only coil for Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 1.5T. 16-element receive only coil for Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

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

Class I — Serious Health HazardOngoing
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...

The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Amoxicillin and Clavulanate Potassium Tablets USP Recalled by Teva...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2024· Beckman Coulter, Inc.

Recalled Item: Dxl 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: The analyzers were built with nonconforming USB cables made with brass...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2024· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Recalled by Zyno Medical LLC Due to Zyno Medical has found...

The Issue: Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Stryker Corporation

Recalled Item: The Non-Sterile Flyte hood covers the user s head and Recalled by Stryker...

The Issue: Expired Products distributed to customers

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Stryker Corporation

Recalled Item: This product is a single use sterile device that is Recalled by Stryker...

The Issue: Expired Products distributed to customers

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings, Inc....

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing