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. 2,609 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,609 in last 12 months

Showing 1090110920 of 28,748 recalls

Medical DeviceOctober 23, 2020· Coloplast Manufacturing US, LLC

Recalled Item: Titan Pump - Product Usage: indicated for male patients suffering Recalled...

The Issue: Potential increased occurrence of pump fracture over the lifetime of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Mako Surgical Corporation

Recalled Item: Mako Integrated Cutting System (MICS) Handpiece Recalled by Mako Surgical...

The Issue: Stryker has discovered a characterization issue associated with the Mako...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to Some...

The Issue: Some electronic components within the generator were equipped with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2020· Viewray, Inc.

Recalled Item: ViewRay MRIdian System: Model No. 10000 Recalled by Viewray, Inc. Due to...

The Issue: There is a potential that components of the receive coil can reach elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2020· Viewray, Inc.

Recalled Item: ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due...

The Issue: There is a potential that components of the receive coil can reach elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone Recalled by...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment beam...

The Issue: Treatment beam information disappears on Treatment Console screen while beam...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone Recalled...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone Recalled...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Ra Medical Systems, Inc.

Recalled Item: DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in Recalled by Ra...

The Issue: Due to footswitch not meeting required specification for protection from...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing