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. 2,483 recalls have been distributed to Kentucky in the last 12 months.
Showing 21401–21420 of 28,748 recalls
Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set Recalled by...
The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...
The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...
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: 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: 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: 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 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: 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: Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is...
The Issue: Contamination of product with possible Bacillus spp
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap...
The Issue: Aesculap Inc. US has initiated a recall on Tibial and Femur extension...
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: 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: Gold Slotted Screw 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: Certain Standard 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: Conical Abutment Gold Standard ZR TM Dental implants Recalled by Biomet 3i,...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Healing Cap 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: Locator Light Retention Replacement Males 4pk 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.