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 861–880 of 51,386 recalls

Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP60. Product Number: M8005A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Nivagen Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP40. Product Number: M8003A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP80. Product Number: M8008A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX550. Product Number: 866066. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX450. Product Number: 866062. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP30. Product Number: M8002A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP2. Product Number: M8102A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Benco dental Graham CHEMICAL CO. Recalled by Novocol Pharmaceutical of...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Lidocaine HCI 2% and Epinephrine 1:100 Recalled by Novocol Pharmaceutical of...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX100. Product Number: 867033. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Aizu Olympus Co., Ltd.

Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...

The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Arise 1000EX mattress Recalled by Stryker Medical Division of...

The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX750. Product Number: 866471. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: OraVerse Recalled by Novocol Pharmaceutical of Canada, Inc. Due to Defective...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 31, 2025· Blonde Beard's

Recalled Item: Blonde Beard's Dojo Asian Wing Sauce Recalled by Blonde Beard's Due to...

The Issue: Undeclared Soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP5. Product Number: M8105A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: darby dental supply Recalled by Novocol Pharmaceutical of Canada, Inc. Due...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund