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. 1,805 recalls have been distributed to Kentucky in the last 12 months.
Showing 36661–36680 of 51,386 recalls
Recalled Item: Baxter INTERLINK System Recalled by Baxter Healthcare Corp. Due to Potential...
The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Source Administration Sets Recalled by Bayer Healthcare Due to The...
The Issue: The firm's investigation of the Medrad Intego indicates that the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corp. Due to Potential...
The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Y-Type Spike Adapter Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BladderScan BVI 9600 Recalled by Verathon, Inc. Due to The firm is providing...
The Issue: The firm is providing customers with an updated Operations and Maintenance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope AVL Video Laryngoscope (AVL) Recalled by Verathon, Inc. Due to...
The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope (GVL) Recalled by Verathon, Inc. Due to...
The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bond Polymer Red Detection DS9390 kits. The common name Recalled by Leica...
The Issue: The Firm informed the importer/distributor, Leica Microsystems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Provide Abutment Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Preformance Post Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Hex Try-in Screw (5 pk) Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locator Extra Light Retention Males 4pk Dental implants Recalled by Biomet...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold -Tite Hexed Retaining Screw Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard Abutment Dental implants Recalled by Biomet 3i, LLC Due to Pouches...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical Abutment Pick-up Coping Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locator Extended Range Males 4pk Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKOplasty Hip Array Kit Laminate 150230 Recalled by Mako Surgical...
The Issue: Stryker Orthpaedics became aware that there is the potential for the 210540...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...
The Issue: Potential for separation of the proximal handle from the shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare PIIC Classic Upgrade Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.