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 7121–7140 of 28,538 recalls
Recalled Item: Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid...
The Issue: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 300 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the...
The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic...
The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Specific Protein- In vitro diagnostic use Recalled by Randox...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SmartPath to Ingenia Elition X MR System Recalled by Philips North...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR 7700 System Recalled by Philips North America Llc Due to Gradient...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ingenia Elition S MR System Recalled by Philips North America Llc...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ingenia Elition X MR System Recalled by Philips North America Llc...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Upgrade to MR 7700 System Recalled by Philips North America Llc Due...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Fetal Spiral Electrode-intended for patients requiring fetal heart...
The Issue: Fetal Spiral Electrode (FSE) spiral tip of the FSE breaking off during use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Chocolate II Agar- IVD for the isolation and cultivation Recalled by...
The Issue: Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica MICROSYSTEMS M530 OHX Recalled by Leica Microsystems, Inc. Due to...
The Issue: There is a potential issue resulting in the Power Supply potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.