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. 2,370 recalls have been distributed to Kansas in the last 12 months.
Showing 721–740 of 50,117 recalls
Recalled Item: Italian Salad Dressing Recalled by VENTURA FOODS LLC Due to Foreign Object...
The Issue: foreign objects (black plastic planting material) in granulated onion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Publix Deli Carolina-Style Mustard BBQ Sauce Recalled by VENTURA FOODS LLC...
The Issue: foreign objects (black plastic planting material) in granulated onion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...
The Issue: Due to a number of modules flashed with a date and time associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100220-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100125-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertraline Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....
The Issue: Defective container - seal not adhering to bottles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemochron Activated Clotting Time Low-Range Test Cuvette Recalled by Accriva...
The Issue: Test cuvettes, used with an assay for monitoring heparin anticoagulation,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100325-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100230-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100425-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100225-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10. Recalled by Cepheid Due to...
The Issue: Product testing did not meet expected stability criteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid. Intra-Aortic Balloon Pump system. Recalled by Datascope...
The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue. Intra-Aortic Balloon Pump system. Recalled by Datascope...
The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX"...
The Issue: Labeling contains claims that are not consistently present.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Recalled...
The Issue: Labeling contains claims that are not consistently present.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Recalled by...
The Issue: Labeling contains claims that are not consistently present.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pollen Allergy Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Recalled...
The Issue: Labeling contains claims that are not consistently present.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.