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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 2301–2320 of 28,748 recalls
Recalled Item: AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXperFD20/15 System Code: (1) 722058 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M12 System Code: (1) 722227 (2) 722231 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 Recalled by PHILIPS...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 System Code: (1) 722038 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 Recalled...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C System Code: (1) 722001 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing device labeling is being updated to strengthen labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...
The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...
The Issue: Potential that the induction seal is not completely sealed to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...
The Issue: Due to manufacturing issue (unintended by-product of the injection molding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...
The Issue: Product complaints were received describing the A820 myPTM app taking longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number:...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.