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. 2,465 recalls have been distributed to Kansas in the last 12 months.
Showing 19821–19840 of 50,117 recalls
Recalled Item: Stryker Pin To Rod Coupling External Fixation System Hoffmann II Recalled by...
The Issue: Pin To Rod Coupling could not clamp the pin and rod as intended
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The products involved are DeWALT laser distance measurers Recalled by...
The Issue: The products are labeled as Class II lasers. However, the level of laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Advanced Recalled by 3M Company - Health Care Business Due to...
The Issue: While the product meets all safety and efficacy criteria, long term exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal KNEE BRACE Recalled by DeRoyal Industries Inc Due to The Warrior...
The Issue: The Warrior Recovery Knee Brace has the potential to come apart due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranitidine Tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 8 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 7 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.