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. 2,522 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,522 in last 12 months

Showing 1760117620 of 50,117 recalls

Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Talladium Inc

Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...

The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2020· ROQUE PLAST, S.A. DE C.V.

Recalled Item: Command Brands GelAnti Bac Instant Hand Sanitizer Recalled by ROQUE PLAST,...

The Issue: CGMP Deviation: Potential contamination with undeclared methanol.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2020· Eosera, Inc.

Recalled Item: Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles...

The Issue: cGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2020· Eosera, Inc.

Recalled Item: Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) Recalled by...

The Issue: cGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2020· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...

The Issue: Subpotent drug: Out of specification for assay at the 15-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2020· Eosera, Inc.

Recalled Item: Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine Recalled by...

The Issue: cGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2020· Eosera, Inc.

Recalled Item: Ear Pain MD Pain Relief Drops For Kids (lidocaine HCl Recalled by Eosera,...

The Issue: cGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...

The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...

The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....

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

Class I — Serious Health HazardOngoing