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. 934 recalls have been distributed to Kentucky in the last 12 months.
Showing 43401–43420 of 51,386 recalls
Recalled Item: Stryker 5.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1.5mm Wire Pass Drill Sterile Product Usage: The devices Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 3.0mm x 3.8mm Neuro Drill Sterile Product Usage: The Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 3.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lindemann Drill Short Recalled by Stryker Instruments Div. of Stryker...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 4.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 6.0mm Egg Bur Sterile Product Usage: The devices are Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1.3mm Wire Pass Drill Sterile Product Usage: The devices Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Wearable Patient Monitor in use with the Philips Recalled by...
The Issue: IntelliVue MX40 (part numbers 865350, 865352) with software revisions B.00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.5mm Round Fluted Bur Soft Touch Sterile Product Usage: Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.0mm Egg Bur Sterile Product Usage: The devices are Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connection QRG for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is Recalled by Brainlab AG...
The Issue: Brainlab Navigation Software Spine & Trauma 3D 2.0/2.1 offers automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stapler Addendum for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche MODULAR ANALYTICS EVO Serum Work Area (SWA) Recalled by Roche...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System...
The Issue: A portion of the BBL Crystal Enteric/Nonfermentor (E/NF) Identification kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 analyzer series Operators Manual Roche cobas Filter label:...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insert for IRK for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vision Troubleshooting Guide for the da Vinci Standard Surgical System...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Manual for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.