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. 2,616 recalls have been distributed to Kansas in the last 12 months.
Showing 4981–5000 of 28,538 recalls
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: 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 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: 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: 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: 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: 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: 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: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
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.
Recalled Item: Baxter Coseal Premix Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
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.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Thru Intraluminal Shunt Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.