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. 2,483 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,483 in last 12 months

Showing 2118121200 of 28,748 recalls

Medical DeviceJanuary 4, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...

The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...

The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2015· Cordis Corporation

Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...

The Issue: Incorrect cannula of the sheath introducer (smaller than intended).

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2015· Leica Microsystems, Inc.

Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...

The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...

The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Pharmacaribe llc

Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...

The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Radiometer America Inc

Recalled Item: AQURE System Recalled by Radiometer America Inc Due to The AQURE System has...

The Issue: The AQURE System has a design error regarding sample type in which sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2015· Phadia Ab

Recalled Item: EliA SmDP Well Recalled by Phadia Ab Due to All equivocal and positive...

The Issue: All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549380 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549470 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549530 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548320 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549540 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548890 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549460 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549500 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548240 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548500 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548460 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548230 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing