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 7021–7040 of 50,117 recalls
Recalled Item: Flow-i C40 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST)...
The Issue: There is the potential for incomplete staple line formation during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eprontia (topiramate) oral solution Recalled by Azurity Pharmaceuticals,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WAVi Research EEG Desktop System is comprised of the WAVi Recalled by WAVi...
The Issue: Following an FDA-issued Warning Letter, the firm requested return of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Distal Cover MAJ-2315 Used with: EVIS EXERA III Recalled by...
The Issue: Single Use Distal Cover MAJ-2315 may unexpectedly detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by...
The Issue: Loss of connectivity between the FlexArm and the Table due to a software issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by...
The Issue: Loss of connectivity between the FlexArm and the Table due to a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0848 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0847 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0846 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0845 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shakespeare's Pizza Recalled by Shakespeare's Pizza, Inc. Due to Undeclared...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shakespeare's Pizza Recalled by Shakespeare's Pizza, Inc. Due to Undeclared...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shakespeare's Pizza Recalled by Shakespeare's Pizza, Inc. Due to Undeclared...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shakespeare's Pizza Recalled by Shakespeare's Pizza, Inc. Due to Undeclared...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terragene Bionova PCD (PCD222-C) Recalled by TERRAGENE S.A. Due to Due to a...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator Recalled by...
The Issue: During internal review of Polaris battery assembly data from the HiPot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Due to If the Patient...
The Issue: If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.