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. 2,646 recalls have been distributed to Kentucky in the last 12 months.
Showing 5581–5600 of 28,748 recalls
Recalled Item: Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System Recalled by...
The Issue: Device packaged inside an incorrect outer box; displaying artwork &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Dry Seal Chest Drains (Express): 4000-100N DRAIN Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drains (Ocean): Products Product Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Dry Suction Water Seal Chest Drains (Oasis): (1)3600-100 DRAIN...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235. PTS-11 versions Recalled by Ion...
The Issue: The patient positioning system can perform motions in unexpected directions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Stat Profile Prime Plus POC Analyzer (CE)-Intended to measure Recalled...
The Issue: Potential risk of reporting erroneous creatinine patient results associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Prime Plus Analyzer -Intended to measure certain gases in...
The Issue: Potential risk of reporting erroneous creatinine patient results associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module 8120 Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCU Recalled by CareFusion 303, Inc. Due to Alaris PCA Module...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Video System Center Model Number CV-190. Intended Recalled by...
The Issue: Certain serial numbers of the CV-190 do not start up properly because parts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptima CMV Quant Assay Recalled by Hologic, Inc. Due to Use of assay along...
The Issue: Use of assay along with plasma specimen may result in error code which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG WALKER FOLDING WALKER WITH WHEELS Utilized as Recalled by Breg Inc Due...
The Issue: Due to walkers not meeting product specifications. Walkers were manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Acrobat-i Vacuum Stabilizer System Intended for use during...
The Issue: Housing Mount Jaw of these devices breaking during normal use and may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 and Astral 150 ventilators Recalled by ResMed Ltd. Due to If...
The Issue: If ventilator is on internal battery, not intended to serve as a primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...
The Issue: Syringe contains conical tip that is not compatible with certain needleless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System Recalled by...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The firm has investigated and confirmed that when DxI 9000 is connected to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.