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. 927 recalls have been distributed to Kansas in the last 12 months.
Showing 45721–45740 of 50,117 recalls
Recalled Item: Mesa EZtest BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for use in...
The Issue: Mesa EZTest , Self-contained steam biological indicator, are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...
The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...
The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...
The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...
The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cleocin Phosphate (clindamycin Injection) Recalled by Pharmacia & Upjohn LLC...
The Issue: Presence of Particulate Matter: Firm is recalling a small number of vials...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Sutureless Pump Connector Revision Kit Recalled by Medtronic...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX Evolution System Recalled by Carestream Health Inc. Due to...
The Issue: Due to potential for an x-ray exposure technique change.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMC Saddle Product Usage: The Ascension CMC is intended to Recalled by...
The Issue: As a result of a quality review, labelling content discrepancies were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic INDURA 1P Intrathecal Catheter Recalled by Medtronic...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU5800 Clinical Chemistry Analyzer with Automation Ready Connection (All...
The Issue: The recall was initiated because Beckman Coulter has identified a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler Set Single Conn./Ext DL Product Number: 050-87216...
The Issue: Cassette may leak during set up or during peritoneal dialysis treatment
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed EL Programmable pumps Recalled by Medtronic...
The Issue: Medtronic is providing Healthcare Professionals with important safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intrathecal Catheter Recalled by Medtronic Neuromodulation Due to...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is providing Healthcare Professionals with important safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intrathecal Catheter Pump Segment Revision Kit Recalled by...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX Instrument Recalled by Becton Dickinson & Co. Due to Electrical power...
The Issue: Electrical power module installed on some in vitro diagnostic instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Recalled by...
The Issue: The firm is initiating a Field Safety Correction for the labeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Vector Distractor Pin Holding Clamp Recalled by Synthes USA HQ, Inc....
The Issue: Synthes is initiating a voluntary Medical Device removal for specified part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.