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 721–740 of 51,386 recalls
Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...
The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm Recalled by C.R....
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...
The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertraline Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....
The Issue: Defective container - seal not adhering to bottles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100425-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100225-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100220-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100325-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100125-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100230-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemochron Activated Clotting Time Low-Range Test Cuvette Recalled by Accriva...
The Issue: Test cuvettes, used with an assay for monitoring heparin anticoagulation,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10. Recalled by Cepheid Due to...
The Issue: Product testing did not meet expected stability criteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue. Intra-Aortic Balloon Pump system. Recalled by Datascope...
The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid. Intra-Aortic Balloon Pump system. Recalled by Datascope...
The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SQ40S Blood Transfusion Filter Recalled by GVS TM, Inc Due to Due to...
The Issue: Due to products being released for distribution prior to completion of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retail Box: Haagen-Dazs mini chocolate dark chocolate ice cream bars...
The Issue: Undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.