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. 1,805 recalls have been distributed to Kansas in the last 12 months.
Showing 31061–31080 of 50,117 recalls
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...
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: Phenytoin 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: 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.
Recalled Item: BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G Recalled by Argon...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An error in NVIDIA GPU (Graphics Processing Unit) card drivers can occur for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT X-Ray Recalled by Philips Electronics North...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance 64 System Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT SP X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN Recalled by Argon Medical...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST NEEDLE 15GA X 2 Intended for the purpose of Recalled by Argon...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Strata II / Strata NSC Valves (includes Burr Hole Recalled by...
The Issue: Medtronic Neurosurgery initiated a recall after receiving five (5) Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Duodenoscope These instruments are intended to provide optical...
The Issue: Pentax initiated a field correction/safety alert for two (2) models of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5...
The Issue: A portion of this lot of blood collection tubes was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.