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 27581–27600 of 50,117 recalls
Recalled Item: BBQ Sauce Recalled by CFS West Holdings Inc Due to Undeclared Egg
The Issue: Products potentially contain undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Texas Roadhouse Barbecue Sauce Recalled by CFS West Holdings Inc Due to...
The Issue: Products potentially contain undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Worcestershire Sauce Recalled by CFS West Holdings Inc Due to...
The Issue: Products potentially contain undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: West Creek Sweet BBQ Sauce Recalled by CFS West Holdings Inc Due to...
The Issue: Products potentially contain undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almonds Covered...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...
The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Mednet(TM) Medication Management Suite 6.1 and 6.21 Recalled by ICU...
The Issue: Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol Recalled by Dr....
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate In 0.9% Sodium Chloride Recalled by Pharmedium Services,...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meclizine hydrochloride tablets USP Recalled by Jubilant Cadista...
The Issue: Marketed without an approved NDA/ANDA: Bottles were released prior to final...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...
The Issue: Report was of an interrupted MR scan after patient complained about acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...
The Issue: L3 has determined in airport environments, there have been several cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...
The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...
The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.