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. 2,386 recalls have been distributed to Kansas in the last 12 months.
Showing 39781–39800 of 50,117 recalls
Recalled Item: iNDiGO capsules Recalled by Detox Transforms Due to Undeclared Phenolphthalein
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BtRiM Max capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROBAR Frosted Peanut Butter BASE Protein Bar Recalled by Probar LLC Due to...
The Issue: PROBAR, LLC has initiated a voluntary recall of its PROBAR Base Frosted...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MAX-TL 9.0 x 7.0 mm Implant Recalled by Southern Implants, Inc Due to Z-MAX...
The Issue: Z-MAX Implant, 9mm diameter, 7mm length labeled package, catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Passport V Monitor Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: An issue has been identified with Passport V Monitors invasive blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use Recalled by...
The Issue: When using the MAKOplasty partial knee Arthroplasty application, the burr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare Corp....
The Issue: Product may have separating or protruding sponges
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 140/175 uL Recalled by Siemens...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 100 uL Recalled by Siemens Healthcare...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 50/60 uL Recalled by Siemens...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORUM Archive and Viewer Recalled by Carl Zeiss Meditec AG Due to Software...
The Issue: Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Raw 100% Organic Sunflower Seeds Recalled by Freeland Foods Inc. Due to...
The Issue: CFIA notified firm of positive finding of Salmonella in Go Raw Spicy Seed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Go Raw Organic Spice Seed Mix Recalled by Freeland Foods Inc. Due to...
The Issue: CFIA notified firm of positive finding of Salmonella in Go Raw Spicy Seed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aquarius iNtuition Client Viewer. Findings Workflow module Recalled by...
The Issue: Software anomaly related to RECIST1.1 target lesion evaluation criteria in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS Oncology Information System Servers Recalled by Siemens...
The Issue: There is a potential safety risk when using LANTIS server software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Catheters and PICCs: Product identification: MCDLTSL24P (SF X...
The Issue: Drug products contained within the kits may have been rendered ineffective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2...
The Issue: A device malfunction may cause the biopsy needle to fail to reach the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.