Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,137 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,137 in last 12 months

Showing 741–760 of 51,386 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: 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: Mycoplasma 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· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Downstream Occlusion alarms may occur during procedures using low flow...

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: Food Intolerance 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· 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: 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: 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: Allergy Test IgE 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: Alcohol (ALC) Test Saliva 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 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
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: 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: 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
FoodNovember 3, 2025· Dreyer's Grand Ice Cream, Inc.

Recalled Item: Retail Box: Haagen-Dazs mini chocolate dark chocolate ice cream bars...

The Issue: Undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
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· GET TESTED INTERNATIONAL AB

Recalled Item: Adrenal 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: Neurotransmitters Plus 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: 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· 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