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. 2,423 recalls have been distributed to Mississippi in the last 12 months.
Showing 37601–37620 of 49,744 recalls
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...
The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lerner Laboratories Mucolexx Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azithromycin 500 mg tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adrucil (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: Black particulate matter was identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KABIVEN [(3.9%) Lipid Injectable Emulsion with (3.1%) Amino Acids and...
The Issue: Labeling: Label Error on Declared Strength: Labeled 3.1% Amino Acids but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Alcon Custom Pak. The Alcon Customer Pak is an Recalled by Alcon...
The Issue: The supplier of the Devon Light Glove, a component of the Alcon Custom PAK,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves:...
The Issue: Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRIT-LINE Blood Chamber- an accessory to the Crit line III- Recalled by...
The Issue: Blood chamber connection leaks during the use of the CRIT-LINE¿ Blood Chamber
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raw Pine Nuts sold in the following brands and package Recalled by Waymouth...
The Issue: Waymouth Farms is recalling Raw Pine Nuts because they have the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EliteCore Full Core Biopsy Device. EliteCore 18G Recalled by Stryker...
The Issue: Potential for the device cannula to overthrow past the intended length.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-fend Recalled by GE Healthcare Due to A potential safety issue due to loss...
The Issue: A potential safety issue due to loss of gas monitoring associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levalbuterol Inhalation Solution Recalled by Cipla Limited Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product is out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alinia (nitazoxanide) Recalled by Romark Laboratories, L.C. Due to Failed...
The Issue: Failed Stability Specifications: Product failed to meet 12 months long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.