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. 2,497 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,497 in last 12 months

Showing 1978119800 of 28,748 recalls

Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products LAC Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Synergetics Inc

Recalled Item: 25 gauge VersaVit 2.0 Vitrectomy Cutter Recalled by Synergetics Inc Due to...

The Issue: Vitrectomy cutters have been found not to be operating within the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products URIC Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Synergetics Inc

Recalled Item: 25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator Recalled by...

The Issue: Vitrectomy cutters have been found not to be operating within the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1265 Blood Gas Analyzer Siemens Material Number (SMN): 10321852...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1260 Blood Gas Analyzer Siemens Material Number (SMN): 10321846...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab 1240 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1245 Blood Gas Analyzer Siemens Material Number (SMN): 10321844...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 400 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 03 ml Squeeze Flush Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: 5 Port OFF Manifold with Transpac IV Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Triple Line SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with SafeSet Reservoir and Blood Sampling Port...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Single Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Reservoir and 2 Blood Sampling...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Blood Sampling Ports Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Bifurcated SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Monitoring Kit with TP4 Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing