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. 2,457 recalls have been distributed to Kentucky in the last 12 months.
Showing 26001–26020 of 28,748 recalls
Recalled Item: ADVIA Centaur Folate (100 Tests) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Calibration failures and/or significant negative shifts in quality control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...
The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...
The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nestle Nutrition Recalled by Nestle HealthCare Nutrition Due to Nestle...
The Issue: Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...
The Issue: Potential for clinical errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRI Cocaine Metabolite Assay Recalled by Microgenics Corp Due to...
The Issue: Surveillance of reagent stability for specific lots of DRI Cocaine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...
The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-Slice CT Scanner System. Used as a whole-body computed Recalled by...
The Issue: A pinch point at the end of the table top can cause injury.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...
The Issue: The firm issued a clinical alert after users reported an issue where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.