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. 1,029 recalls have been distributed to Kentucky in the last 12 months.
Showing 21061–21080 of 51,386 recalls
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...
The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium/ Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sacharate Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium /Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major Infants' Gas Relief Drops Recalled by GCP Laboratories Inc Due to...
The Issue: Microbial Contamination of Non-Sterile Product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: In-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Diff Dropper Recalled by Biomedical Polymers, Inc. Due to The metal...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor Recalled by...
The Issue: Eversense Sensors have prematurely stopped functioning due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemo-Drop Blood Dispenser Recalled by Biomedical Polymers, Inc. Due to The...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...
The Issue: Incomplete seal and premature expiration of individually packaged Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.