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. 1,805 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,805 in last 12 months

Showing 3778137800 of 51,386 recalls

DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Methyldrene Original 25 Ephedra ECA Stack Extra-Potent Fat Burner Dietary...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: Rusch Flexi-slip tracheal tube Stylet Recalled by Teleflex Medical Due to...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip Recalled by...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit Tubing Pack P/N: 66041-1 Terumo...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack with...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Pediatric Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Mislabeling

The Issue: Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· DJO, LLC

Recalled Item: Monode Recalled by DJO, LLC Due to Overheating and burning of the wire...

The Issue: Overheating and burning of the wire insulation inside the applicator.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 Recalled by Olympus...

The Issue: Insufficient information for specific cleaning accessories used for the...

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

Class II — Potential Health HazardOngoing
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Recalled by...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: HEParin Sodium 0.5 USP UNITS/mL in 0.225% SODIUM CHLORIDE Recalled by...

The Issue: Stability Data Does Not Support Expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: Atropine Sulfate Injection Solution Recalled by Cantrell Drug Company Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund