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. 2,498 recalls have been distributed to Kentucky in the last 12 months.
Showing 19101–19120 of 28,748 recalls
Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens initiated a corrective action to address two possible, mutually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N...
The Issue: Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products UPRO Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: There is a potential for variable negatively and positively biased urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/Q.zen Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens initiated a corrective action to address two possible, mutually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...
The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...
The Issue: Edits to Particle field definition parameters may not be saved when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology 12.2 - Picture Archive Communication System (PACS)...
The Issue: Issue for customers that use an EMR login or legacy web URL login or legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...
The Issue: Reunion TSA Peg Alignment Sound broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.