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. 2,423 recalls have been distributed to Kansas in the last 12 months.
Showing 25921–25940 of 50,117 recalls
Recalled Item: CT Goldseal Optima CT 600 Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima CT 540 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allergan Taytulla Softgel Capsules Recalled by Allergan, PLC. Due to...
The Issue: Contraceptive Tablets Out of Sequence.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Recalled by Steris...
The Issue: The firm has become aware that the Reliance 1227 Cart and Utensil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: This email is to provide notification that, due to a software bug that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: simply delicious Divvies SEMI-SWEET PEPPERMINT BARS made to share CHOCOLATE...
The Issue: Product may contain traces of milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol Recalled by Lake...
The Issue: Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANSYS MLP/DLP Recalled by NewDeal SA Due to Use of the impacted product...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNI-CP Recalled by NewDeal SA Due to Use of the impacted product may cause a...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.