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. 2,095 recalls have been distributed to Kentucky in the last 12 months.
Showing 4081–4100 of 28,748 recalls
Recalled Item: Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate2 8F x 85cm Recalled by Stryker Neurovascular Due to Neurovascular...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Pro 14 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGIFOAM" Absorbable Gelatin Powder Kit Recalled by Ethicon, Inc. Due to...
The Issue: Some applicator tips from these lots had open seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well. Intended to be Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well and 2 inch Recalled by Mirion...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance Recalled by...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Independent Medical Co-op Inc. Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System. Intended to be used to Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE Recalled by MEDLINE...
The Issue: It has been identified that testing documentation does not support that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) Recalled...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity and Clarity Diagnostics LLC Recalled by Wondfo USA Co Ltd Due to...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preview Strep A Recalled by Wondfo USA Co Ltd Due to Wondfo USA has...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX...
The Issue: Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.