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. 1,129 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,129 in last 12 months

Showing 1641–1660 of 50,117 recalls

Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Philips Medical Systems Nederland B.V.

Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...

The Issue: Software issue that results in the display of outdated information.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 2023B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Greiner Bio-One North America, Inc.

Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...

The Issue: Blood collection tubes were manufactured with the label applied too high on...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2025· Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...

The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...

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

Class III — Low RiskOngoing
Medical DeviceAugust 6, 2025· Cepheid

Recalled Item: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code:...

The Issue: As a result of Post-Market half-time stability testing, false negative test...

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED PHYTOSTEROL 99%)...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild...

The Issue: Unapproved Drug Claims.

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

Class III — Low RiskOngoing
Refund