Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,598 recalls have been distributed to Kansas in the last 12 months.
Showing 8181–8200 of 28,538 recalls
Recalled Item: progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner...
The Issue: Inner pouch seal may be inadequate resulting in lack of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Devices...
The Issue: Devices were subject to unapproved rework processes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Medtronic Inc Due to The pump...
The Issue: The pump may have a welding defect that can lead the pump to malfunction....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 ToRC IgM Reagent Pack Recalled by Bio-Rad Laboratories, Inc....
The Issue: Performance concerns for the CMV IgM analyte. Analyte has demonstrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe Recalled by...
The Issue: Patient chart label contains incorrect Part Number and volume amount.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - automated Recalled by Siemens Healthcare...
The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - automated Recalled by Siemens Healthcare...
The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320 WUWD Series Washer Disinfector-For use as a multi-chamber...
The Issue: Verification of installation not documented or may be incomplete, could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...
The Issue: Siemens has become aware of three potential software issues with AXIOM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe...
The Issue: Product labeled incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320-2 CHAMBER WU Series Washer Disinfector- For Use as Recalled by...
The Issue: Verification of installation not documented or may be incomplete, could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crome Models loaded with CareLink SmartSync Device Manager application...
The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Models loaded with CareLink SmartSync Device Manager application...
The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane -angiography systems developed for single and biplane...
The Issue: if the protective earth is interrupted and an additional fault leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor-angiography systems developed for single and biplane...
The Issue: if the protective earth is interrupted and an additional fault leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...
The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...
The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Gibeck Humid-Vent 2S Flex DC Recalled by TELEFLEX MEDICAL INC Due to...
The Issue: Reports received of torn corrugated breathing tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports...
The Issue: Reports received of torn corrugated breathing tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer Recalled by Radiometer Medical ApS Due to Arterial Blood Sampler...
The Issue: Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.