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. 2,602 recalls have been distributed to Kentucky in the last 12 months.
Showing 13121–13140 of 28,748 recalls
Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...
The Issue: Due to low Quality Control recovery and invalid Calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...
The Issue: Due to low Quality Control recovery and invalid Calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...
The Issue: The firm received a report of an atypical dataset being generated. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...
The Issue: The instrument holder may be sent on a trajectory that is not within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...
The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...
The Issue: The recall is being conducted due to a potential defective component on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...
The Issue: The touchpad may not work properly after cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron Systems Opiate 2000 ng Reagent (OP2 1 x 250) Recalled by Beckman...
The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opiate 300 Ng Reagent (OP 1 X 250) for use Recalled by Beckman Coulter Inc....
The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate 300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.