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. 2,341 recalls have been distributed to Kansas in the last 12 months.
Showing 43301–43320 of 50,117 recalls
Recalled Item: Medtronic Select CAP Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2055: Prevena Customizable Dressing 5-Pack Product Usage: The Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...
The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intersept Custom Tubing Pack which contain Select 3D or Recalled...
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelzone Shoulder Sleeve Recalled by Implantech Associates Inc Due to...
The Issue: Implantech initiated the voluntary recall of Gelzone Shoulder Sleever,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gano C'Real Spirulina Recalled by Gano Excel USA Inc Due to Undeclared Wheat
The Issue: Gano Excel USA is recalling the C'Real Spirulina because it contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GREENSTONE BRAND fluconazole for Oral Suspension Recalled by Pfizer Inc. Due...
The Issue: Defective Container: Tamper evident ring failures discovered on some bottles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxcarbazepine Tablets Recalled by Caraco Pharmaceutical Laboratories Ltd....
The Issue: Failed Tablet Specifications: Broken Tablets Present.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Cream USP Recalled by Fougera Pharmaceuticals Inc....
The Issue: Labeling: Label Error on Declared Strength: There is a misprint on the end...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carisoprodol Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurity/degradation Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin HCl Extended-Release Tablets Recalled by Caraco Pharmaceutical...
The Issue: Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the...
The Issue: Unapproved material used by vendor in subset of shorts causing them to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Picture Archiving and Communication System (PACS). Model...
The Issue: Potential patient data mixup. Improper error handling could allow for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.2 mm Guide Wire 400mm. Used for guiding the Recalled by Synthes,...
The Issue: Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems, Inc. Due to Cardio vascular Systems...
The Issue: Cardio vascular Systems Inc. has initiated a recall to request the immediate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes...
The Issue: Certain modules containing the Synthes Small Notch Titanium Reconstructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product did not meet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product did not meet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pringles Recalled by Kellogg Company Due to Undeclared Milk
The Issue: Undeclared milk, an allergen
Recommended Action: Do not consume. Return to store for a refund or discard.