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. 2,423 recalls have been distributed to Kansas in the last 12 months.
Showing 26741–26760 of 50,117 recalls
Recalled Item: Life Change Fat Burner Recalled by Get The Tea Due to Get The Tea is...
The Issue: Get The Tea is notifying customers that Life Change Fat Burners contain soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Testosterzone 180 count bottle packaged in an amber plastic bottle Recalled...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thyroid Resilience 120 count bottle packaged in an amber plastic Recalled by...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pink flexible Recalled by Ikea North America Srvcs Inc Due to Possible Pest...
The Issue: Possible Pest Contamination at production facility.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cobas b 221<4>Roche OMNI S4 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and Recalled...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<6>Roche OMNI S6 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221 AutoQC Module Complete Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 125II Assay Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Upon dilution, some patient samples may exhibit over-recovery outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution Recalled by Draegar...
The Issue: The invasive pressure visual and audible alarms may not activate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-2.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clariti 1 day/Fresh Day 90 pack (-1.00) Recalled by CooperVision Inc. Due to...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-4.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clariti 1 day (-1.25) 90 pack Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 with 4.1.7 XX026 software version model number 728231 Recalled...
The Issue: Surview scan with tube current lower than 30 mA is unable to be initialized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.