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. 1,839 recalls have been distributed to Kansas in the last 12 months.
Showing 27281–27300 of 28,538 recalls
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...
The Issue: It was found that there is a problem with the LCD monitor used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression MRI Patient Monitoring System. The Expression...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...
The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Discovery NM/CT670 Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Enteralite Ambulatory Feeding Pumps Recalled by MOOG Medical...
The Issue: The firm is adding an addendum to the operator's manual for Infinity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: Recalled by...
The Issue: There is a small risk of a leak in Cycler Sets and if the Cycler Set is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker Model 6390 Recalled by Stryker Medical Division of Stryker...
The Issue: Model 6390 Power-LOAD systems built between September 12, 2012 and September...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...
The Issue: Firm has received reports from customers that the small pins at the bottom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAVIG PORTEGRA 2 system operated in conjuction with a Siemens Recalled by...
The Issue: A particular component may not have been fitted during the installation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.