Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,365 recalls have been distributed to Mississippi in the last 12 months.
Showing 45401–45420 of 49,744 recalls
Recalled Item: Invacare Power Wheelchair Recalled by Invacare Corporation Due to Unintended...
The Issue: Unintended slowing or deceleration, and on rare occasion, unanticipated and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesa Smart-Read EZTEST BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for...
The Issue: Self-contained steam biological indicator, are recalled because Mesa...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: ExactaMix 1200 and 2400 Compounders. Used as an automated pumping Recalled...
The Issue: Baxter Healthcare is recalling certain ExactaMix automated compounding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respironics V60 Ventilator Recalled by Respironics California Inc Due to...
The Issue: Respironics California, Inc. has initiated a recall on the V60 ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Deltran Disposable Pressure Transducer Kit (DPT Kit) Extracorporeal...
The Issue: Utah Medical Products, Inc. is recalling certain Deltran Disposable Pressure...
Recommended Action: Stop using. Contact the manufacturer or your 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: 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: 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 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 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: 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: 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 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 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: 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: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. (Pfizer) is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.