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. 2,440 recalls have been distributed to Kansas in the last 12 months.
Showing 23701–23720 of 50,117 recalls
Recalled Item: Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1 ounce Recalled...
The Issue: Product tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for...
The Issue: Insufficient seal on the sterile barrier of the device, compromising the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion Pack Recalled by LivaNova USA Due to 4-way stopcocks and stopcock...
The Issue: 4-way stopcocks and stopcock manifold assembled in certain perfusion tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Stat Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by AMERICAN...
The Issue: Cross contamination with other products: This sub-recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equi-Soft Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ERBITUX CETUXIMAB Injection Recalled by Eli Lilly & Co Due to Labeling:...
The Issue: Labeling: Missing label; potential for missing primary container label on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 09076 / Recalled...
The Issue: Possible contamination with cleaning chemicals.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz. Recalled by...
The Issue: One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled...
The Issue: Unintentional U-Arm movement
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips...
The Issue: kV/mA lockin not functioning as specified which may result in the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Volcano FFR software used in the following systems connected...
The Issue: Interoperability issue that affects certain systems that use the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clopidogrel Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Out-of-Specification results were observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Stability Specifications: Out-of-Specification results obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...
The Issue: Presence of foreign substance: Product found to contain metal particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 100 table Recalled by Deerfield Imaging, Inc. Due to Table may...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 300 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...
The Issue: Cosmetic imperfections on the surface of some lenses.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.