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. 1,726 recalls have been distributed to Kentucky in the last 12 months.
Showing 46241–46260 of 51,386 recalls
Recalled Item: Lidocaine Hydrochloride 2% and Epinephrine 1:100 Recalled by Novocol...
The Issue: Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CARBOplatin Injection Recalled by Teva Pharmaceuticals USA, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: The required reduction of endotoxin was not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens EasyLink Informatics System V4.0/V5 Siemens Recalled by Siemens...
The Issue: May not perform as intended under certain conditions, causing the release of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cypher MIS Screw System Recalled by Ebi, Llc Due to Several complaints were...
The Issue: Several complaints were reported to exhibit screw head splay in the Cypher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument Sternal Zip Flex System intended for use...
The Issue: When using the 1st generation Zip Fix Application Instrument it is possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (6 units) Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (1 unit) Recalled by Codman & Shurtleff, Inc. Due to Drug flow...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products...
The Issue: Following the identification of the disassociation of an impactor tip during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steinmann Pin Recalled by MicroAire Surgical Instruments, LLC Due to A...
The Issue: A medical device used in surgical procedures was packaged in a pouch in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for...
The Issue: Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T8 REMOVAL HEAD Recalled by Medtronic Sofamor Danek USA Inc Due to One lot...
The Issue: One lot of the T8 Removal Head had incorrect hardness specification, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular...
The Issue: Due to a labeling error related to the conversion of the inner diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon 14 Microbore Extension Set with Bionector Recalled by Churchill...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120/2120i Hematology Systems with ADVIA Autoslide connected to it...
The Issue: Siemens determined that if an autosampler rack jam error occurs during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.