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. 2,555 recalls have been distributed to Kentucky in the last 12 months.
Showing 16501–16520 of 28,748 recalls
Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...
The Issue: There is a potential for the connection screw of the stem extractor to break.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conversion SmarthPath to dStream for 1.5T Recalled by Philips Electronics...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System Recalled by Terumo Cardiovascular...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 0.5T Standard Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...
The Issue: The product label has missing information, such as the lot number and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T Recalled by Philips Electronics North America Corporation Due...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.