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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 1961–1980 of 51,386 recalls
Recalled Item: Vercise Deep Brain Stimulation Systems Surgical Implant Manual Recalled by...
The Issue: Wire break(s) have occurred in rechargeable deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Medline General Surgery Tray is customized to meet requirements Recalled...
The Issue: Affected kits contain recalled Stryker Color Cuff Sterile Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burr Hole Cover Kit Recalled by Boston Scientific Neuromodulation...
The Issue: Resistance and difficulties could occur while closing the retaining clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Infusion Sets Recalled by CareFusion 303, Inc. Due to...
The Issue: Infusion pump module used with compatible pump infusion sets may perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Module Model Recalled by CareFusion 303, Inc. Due to Infusion...
The Issue: Infusion pump module used with compatible pump infusion sets may perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J. Higgs Potato Chip Mix Recalled by Saratoga Potato Chips LLC Due to...
The Issue: undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good Neighbor Pharmacy Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ReliOn Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Subpotent...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RITE AID PHARMACY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: H-E-B Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Subpotent Drug-...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent...
The Issue: Certain batches are being removed due to an increase in complaints received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card [25pk]. Material Number: 10736515. Recalled by...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: spike of the cap becomes lodged in the nozzle of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: C5-2 Lumify Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSDUCER L12-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.