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. 931 recalls have been distributed to Kentucky in the last 12 months.
Showing 47501–47520 of 51,386 recalls
Recalled Item: JaDera Recalled by Dolphin Intertrade Corporation Due to Undeclared Sibutramine
The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate; lot being recalled as a precaution due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Sandoz Incorporated Due to Presence of...
The Issue: Presence of Particulate Matter: Found during examination of retention samples.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...
The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...
The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...
The Issue: There is a possibility that the pump head was not shipped in the locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunny Sea Sardines in Tomato Sauce Recalled by Golden Beach Inc Due to...
The Issue: Golden Beach Inc. is recalling Sunny Sea Sardines in Tomato Sauce for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....
The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...
The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...
The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...
The Issue: Cross contamination with other products: Belladonna Alkaloids with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...
The Issue: Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.