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. 2,652 recalls have been distributed to Kentucky in the last 12 months.
Showing 5001–5020 of 28,748 recalls
Recalled Item: Flow-i C30 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C40 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrainFeedback Pro 2 Device - is intended as an instrument Recalled by RONAN...
The Issue: Neurofeedback systems removed due to missing design and development...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAVi Research EEG Desktop System is comprised of the WAVi Recalled by WAVi...
The Issue: Following an FDA-issued Warning Letter, the firm requested return of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0848 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by...
The Issue: Loss of connectivity between the FlexArm and the Table due to a software issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0845 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Distal Cover MAJ-2315 Used with: EVIS EXERA III Recalled by...
The Issue: Single Use Distal Cover MAJ-2315 may unexpectedly detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0847 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by...
The Issue: Loss of connectivity between the FlexArm and the Table due to a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0846 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator Recalled by...
The Issue: During internal review of Polaris battery assembly data from the HiPot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Due to If the Patient...
The Issue: If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terragene Bionova PCD (PCD222-C) Recalled by TERRAGENE S.A. Due to Due to a...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floseal Hemostatic Matrix Fast Prep Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.