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. 2,637 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,637 in last 12 months

Showing 541560 of 28,538 recalls

Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Allergy test Small Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Vitamin D-Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Pollen Allergy Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Candida Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: GI Microbiome Profile XL Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: 8 in 1 STI Test Kit Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Recalled...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Food Intolerance Test Medium Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Fresenius Kabi USA, LLC

Recalled Item: IVENIX INFUSION SYSTEM Recalled by Fresenius Kabi USA, LLC Due to Incorrect...

The Issue: Incorrect assembly of specific lot of LVP Primary Administration Set that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Heavy Metals Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Recalled...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Organic Acids Profile Test Large Recalled by GET TESTED INTERNATIONAL AB Due...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Urinary Tract Infection Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Lactose Intolerance Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Akkermansia Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX"...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing