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. 2,522 recalls have been distributed to Kansas in the last 12 months.
Showing 17481–17500 of 50,117 recalls
Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...
The Issue: Subpotent Drug: FDA analysis found product to be subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...
The Issue: Subpotent Drug: FDA analysis found product to be subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...
The Issue: Subpotent Drug: FDA analysis found product to be subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...
The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM HER-2/neu (H2n) assay Recalled by Siemens Healthcare...
The Issue: Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquas PowerFlow Tube Set - Product Usage: The device delivers Recalled by...
The Issue: The product design incorporating a motor driven impeller pump powered by one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32 Recalled...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32 Recalled...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strides Pharma Inc.Potassium Chloride Extended-Release Tablets Recalled by...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...
The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...
The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Sub-Potent Drug: Out of specification test results for potency (below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...
The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...
The Issue: The third-party brand latex micro surgical gloves packaged within specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.