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 31041–31060 of 50,117 recalls
Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...
The Issue: Potential glass inclusion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...
The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Drape Recalled by Covidien LLC Due to Sterility compromised...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) Recalled...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW¿ Multi-Food 1 Tablets Recalled by NOW Foods Due to Product's supplement...
The Issue: Product's supplement fact panel incorrectly states that the product contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pizza Hut Creamy Alfredo sauce Recalled by Yum Retaurants International Due...
The Issue: Foreign object in alfredo sauce. Likely flexible plastic.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CaviWipes1 Extra Large Recalled by Metrex Research, LLC. Due to Metrex is...
The Issue: Metrex is recalling the CaviWipes Extra Large because they may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp....
The Issue: Posterior tibial fractures have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR450 The systems are whole body magnetic resonance scanners...
The Issue: Potential safety issue with the patient bore heating on the Discovery MR450...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcipotriene Cream 0.0005% Recalled by LEO PHARMA INC Due to Undeclared...
The Issue: Incorrect/Undeclared excipients: inadvertent omission of a drug excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: glipiZIDE Extended-Release Tablets Recalled by Mylan Pharmaceuticals Inc....
The Issue: Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Oral Solution Recalled by VistaPharm, Inc. Due to...
The Issue: Defective Container: Leakage of unit dose cups that may occur at the seal.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoclopramide Oral Solution Recalled by VistaPharm, Inc. Due to CGMP...
The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...
The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...
The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.