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. 2,566 recalls have been distributed to Kansas in the last 12 months.
Showing 11941–11960 of 50,117 recalls
Recalled Item: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry...
The Issue: These products are being recalled due to the potential of leakage from the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry...
The Issue: The third party contract manufacturer used a dextrose ingredient derived...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ambu VivaSight 2 DLT Recalled by Ambu Inc. Due to Firm has received...
The Issue: Firm has received complaints on the device concerning leak/rupture of either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Microcatheter product label on the carton is missing the microcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627 Recalled...
The Issue: Milk contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 710-5364 Recalled...
The Issue: Milk contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Service manuals for the CT Recalled by GE Healthcare, LLC Due to As a result...
The Issue: As a result of unclear guidance in the service manual, the table can drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YelloPort Elite Universal Seal. For use in laparoscopic procedures. Recalled...
The Issue: There is the potential that YelloPort Elite Universal Seals packaging may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...
The Issue: A forced shutdown of one of the processors did not generate a watch dog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...
The Issue: The instrument is incorrectly color coded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...
The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...
The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...
The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...
The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...
The Issue: An issue with propagation of treatment course information from RayStation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card 25 Test Cards/box. In vitro diagnostic Recalled by...
The Issue: Discrepant (low bias) pO2 results, could be an incorrect diagnosis of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...
The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to The...
The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...
The Issue: SE primer may be missing some or all of the resin portion of the chemistry....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...
The Issue: The product was potentially exposed to below-recommended storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.