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. 1,958 recalls have been distributed to Kansas in the last 12 months.
Showing 13481–13500 of 28,538 recalls
Recalled Item: A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire...
The Issue: Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norm-O-Temp model 111Z Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...
The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.