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. 2,335 recalls have been distributed to Kansas in the last 12 months.
Showing 45401–45420 of 50,117 recalls
Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...
The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...
The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silver Sword capsules Recalled by Fabscout Entertainment, Inc Due to...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clalis capsules Recalled by Fabscout Entertainment, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...
The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed customer report of visible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...
The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...
The Issue: Subpotent drug: Avobenzone 3%, one of the active sunscreen ingredients may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...
The Issue: The product was registered and distributed as a Class I medical device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...
The Issue: High inlet water pressure beyond specification and the solenoid valve does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...
The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...
The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens issued a customer safety advisory notice and field safety corrective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latanoprost Ophthalmic Solution Recalled by Apotex Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: Failed at expiry for Preservative...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...
The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...
The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....
The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxytocin Injection Recalled by Fresenius Kabi USA, LLC Due to Subpotent...
The Issue: Subpotent Drug; 15-month stability test station
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.