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. 1,947 recalls have been distributed to Kansas in the last 12 months.
Showing 14941–14960 of 50,117 recalls
Recalled Item: 1. Cahills Ireland Original Irish Porter 5lbs.Waxed Deli Wheel 2. Recalled...
The Issue: Cheese may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lidl Preferred Selection-Red Wine Cheddar - 7 oz. Recalled by CAHILLS FARM...
The Issue: Cheese may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment PCA Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment MU Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment WP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment SP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment NP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment SU Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...
The Issue: Due to potential performance issues with software version 3.2.3 and earlier....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norton Arm Kit Recalled by Aspen Surgical Products, Inc. Due to Affected...
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marco Shoulder Stabilization Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jessie Sterile Arm Suspension Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The...
The Issue: The kit contains the wrong vial tray in the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDI Povidone-Iodine Cleansing Scrub Swabstick (1's) Recalled by Professional...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.