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. 2,636 recalls have been distributed to Kansas in the last 12 months.
Showing 2341–2360 of 50,117 recalls
Recalled Item: Contamac Recalled by Contamac Solutions, Inc. Due to Contact lens insertion...
The Issue: Contact lens insertion solution may lack sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airsupra (albuterol and budesonide) inhalation aerosol Recalled by...
The Issue: Defective delivery system
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Celecoxib Capsules Recalled by AvKARE Due to Presence of Foreign...
The Issue: Presence of Foreign Tablets/Capsules: manufacturer recalled because one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allon 2001. Part Number: 200-00263 Recalled by Belmont Instrument LLC Due to...
The Issue: An investigation into a report of the patient wrap (ThermoWrap), used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Evolution Upgrade 3.0T Recalled by Philips North America Llc...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 3.0T CX Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T CX Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: MR 7700 Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Elition X Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 3.0T Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T S Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for 3.0T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.