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. 1,103 recalls have been distributed to Kansas in the last 12 months.
Showing 3921–3940 of 50,117 recalls
Recalled Item: BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Single User Software Version or Model: 441007 Catalog Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number:...
The Issue: High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...
The Issue: Recalled lot does not meet specification and has reported incidents of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regadenoson Injection Recalled by Baxter Healthcare Corporation Due to...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules Recalled...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IBU (ibuprofen) 600 mg tablets Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIORAPTOR Suture Anchors. Tendon/ligament Recalled by Smith & Nephew Inc....
The Issue: Sterile barrier breach due to inadequate packaging design that could not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Control Pump Recalled by Boston Scientific...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a...
The Issue: Due to incorrect labels applied to devices during servicing. Labels contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy bronchoscope (Product GALB-001) used with Instructions for use...
The Issue: Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.