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. 2,639 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,639 in last 12 months

Showing 66416660 of 28,748 recalls

Medical DeviceApril 6, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Steam Chemical Integrators Recalled by 3M Company - Health Care...

The Issue: 3M Attest Steam Chemical Integrators with dates of manufacture between...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Fisher Wallace Laboratories Inc.

Recalled Item: Fisher Wallace Stimulator Models FW-100 and FW-200 Recalled by Fisher...

The Issue: If the batteries are installed incorrectly, the product may overheat,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Hiossen Inc.

Recalled Item: ET III Nano-HA fixture System ET NH Dental Implant Model Recalled by Hiossen...

The Issue: Mis-labeled length of the dental implant on the Recall Implant's package....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Steam Chemical Integrators Recalled by 3M Company - Health Care...

The Issue: 3M Attest Steam Chemical Integrators with dates of manufacture between...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to an automated dispensing cabinet software issue, when a medication...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Illumina, Inc.

Recalled Item: MiSeq Dx Instrument Recalled by Illumina, Inc. Due to Cybersecurity...

The Issue: Cybersecurity vulnerability concerning the software used for sequencing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Karl Storz Endoscopy

Recalled Item: KARL STORZ Radel Sterilization Trays Recalled by Karl Storz Endoscopy Due to...

The Issue: Plastic sterilization trays used to encase and protect medical devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Illumina, Inc.

Recalled Item: NextSeq 550Dx Instrument Recalled by Illumina, Inc. Due to Cybersecurity...

The Issue: Cybersecurity vulnerability concerning the software used for sequencing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica¿ CH Toxicology...

The Issue: Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry ToxAmmonia Calibrator- In vitro diagnostic use in the...

The Issue: Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Double Swivel Elbow Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...

The Issue: Automated dispensing cabinet software is experiencing: 1) ES device download...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Infinity M300 and M300+ Recalled by Draeger Medical Systems, Inc....

The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Infinity CentralStation (ICS) Recalled by Draeger Medical Systems,...

The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2023· GRAMERCY EXTREMITY ORTHOPEDICS

Recalled Item: GEO Instrument Kit for EPS Plate Recalled by GRAMERCY EXTREMITY ORTHOPEDICS...

The Issue: Instrument Kits for EPS plates may contain drill guides with incorrect drill...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing