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. 2,656 recalls have been distributed to Kentucky in the last 12 months.
Showing 3821–3840 of 51,386 recalls
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Recalled...
The Issue: Increase in complaints associated with a molding defect within the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aerin Medical VivAer Stylus Recalled by Aerin Medical, Inc. Due to Some...
The Issue: Some units in a single production lot were programmed incorrectly which will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST REPROCESSED BRUNS CURETTE #00 (BC00) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Flex reagent cartridge Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics is recalling two lots of their Dimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500) Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin Chewable tablet 81 mg Recalled by Safecor Health, LLC Due to cGMP...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Carbonate Chewable 500 mg Recalled by Safecor Health, LLC Due to...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docusate Sodium 250 mg Recalled by Safecor Health, LLC Due to cGMP...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin B1 Recalled by Safecor Health, LLC Due to cGMP Deviations:...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin D3 Recalled by Safecor Health, LLC Due to cGMP Deviations:...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1....
The Issue: Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.