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 27781–27800 of 50,117 recalls
Recalled Item: Birds Eye Baby Sweet Peas Recalled by Pinnacle Food Group, Llc Due to...
The Issue: Product has the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate 2.0 mEq/L Recalled by Fresenius Medical...
The Issue: The label specifies the potassium concentration is 2.0 mEq/L. Some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer performs three methods of...
The Issue: The firm has become aware of a potential issue that may affect the mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magstim Rapid Therapy System consisting of: Rapid Mainframe Recalled by The...
The Issue: Users manuals not supplied with 4800-00T US Rapid Therapy System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) Recalled...
The Issue: Correction to update sterilizer software to prohibit the use of expired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous...
The Issue: A specific lot of the FlexFlowTM Venous Cannula, 200-200, is being recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...
The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Recalled...
The Issue: There have been reported incidents of fluid leaks at the luer connection....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System...
The Issue: A faulty footswitch may result in unintended ultrasonic fragmentation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.