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. 2,386 recalls have been distributed to Kansas in the last 12 months.
Showing 37241–37260 of 50,117 recalls
Recalled Item: METHYLCOBALAMIN MDV Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADRUCIL (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: silcone rubber and fluorouracil crystals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed...
The Issue: Failed Dissolution Testing: Failed 24 month dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nisoldipine Extended Release Tablets Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray...
The Issue: Defective Delivery System: Inhalers do not spray properly, emitting either...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...
The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC) Recalled by...
The Issue: customers are receiving a high number of Abnormal Assay Errors or are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips GoSafe Mobile Help Button Recalled by Lifeline Systems, Incorporated...
The Issue: Irregular battery disconnection resulted in issues with Mobile Health Button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Pioneer Plus Re-Entry Catheter Recalled by Volcano Corporation Due...
The Issue: Due to a manufacturing defect, there is the possibility that a small wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare TraumaDiagnost Recalled by Philips Electronics North...
The Issue: If arm is not fastened securely it could fall down.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft...
The Issue: Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...
The Issue: The end cap may loosen and detach making the instrument non-functional. No...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER ISOTON 4 Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...
The Issue: Channel Error code is displayed on the PC unit with an audio and visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that...
The Issue: The devices that included the OVAR research test were not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KellBran" CANDIES Recalled by Kellbran Candies and Snacks Inc Due to...
The Issue: The firm was notified by the Ohio Dept. of Agriculture of possible...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Verapamil Hydrochloride Extended-Release tablets Recalled by Apotex Inc. Due...
The Issue: Failed Dissolution Specification: One lot of product did not meet the first...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.