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. 2,639 recalls have been distributed to Kentucky in the last 12 months.
Showing 6301–6320 of 28,748 recalls
Recalled Item: BEQ-HMO 50000-USA/ QUADROX-i Small Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX -i Neonatal Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iD Pediatric Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HMOD70000-USA/QUADROX-iD Recalled by Maquet Medical Systems USA Due to...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to Product packaging...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HMO 71000-USA /QUADROX-i Adult Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HMOD 70000-USA/QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling
The Issue: Devices were mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...
The Issue: A firmware error may lead to an incorrect association of test result(s) to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...
The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...
The Issue: Medtronic has identified that the logfiles downloaded from the recently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Always-On Tip Tracked Instruments (SPiN Drive instruments) Triple Needle...
The Issue: Electromagnetic (EM) sensor tracking malfunction impacts the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.