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. 2,457 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,457 in last 12 months

Showing 2518125200 of 28,748 recalls

Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 10" (25 cm) Appx 2.9 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 6.5" (16.5 cm) Appx 0.30 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 120" 10 Drop Primary Set w/2 BCV-CLAVE¿ Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 10" (25 cm) Appx 0.38 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.26 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 13" Smallbore Ext Set w/4 Gang 4-Way Stopcock w/Baseplate Recalled by ICU...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2013· Mckesson Information Solutions LLC

Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...

The Issue: Images may be archived to an incorrect or invalid archive location resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...

The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...

The Issue: The locking mechanism that is intended to hold the control panel in a fixed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Perrigo Diabetes Care

Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...

The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Zeiss, Carl Inc

Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...

The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...

The Issue: There is a potential for communication loss associated with the F5-01 Frame...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Optimedica Corporation

Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...

The Issue: Potential for unexpected heating of the transformer mounting bolt located...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing