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. 2,438 recalls have been distributed to Mississippi in the last 12 months.
Showing 34341–34360 of 49,744 recalls
Recalled Item: Medtronic Custom Perfusion Tubing Pack Recalled by Medtronic Perfusion...
The Issue: Medtronic is notifying customers who have or may receive specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...
The Issue: The battery capacity of the optional PS500 power supply unit for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...
The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...
The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Diacetate Injectable Suspension Recalled by Isomeric Pharmacy...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...
The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lysander's Premium Teriyaki Marinade Recalled by Geneva Foods, LLC Due to...
The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lysander's All Natural Spicy Bourbon Flavor Rub Recalled by Geneva Foods,...
The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lysander's All Natural Bourbon Flavor Rub Recalled by Geneva Foods, LLC Due...
The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge FlexConnect software Recalled by Merge Healthcare, Inc. Due to...
The Issue: Communication protocols interfacing with the affected software version with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...
The Issue: The software was not presenting the PURE filter user interface message on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is an integrated Recalled...
The Issue: Patient information in the header is only found on the first page of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access used with Merge PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Product was distributed under the AMICAS label Recalled...
The Issue: The patient name in the Halo title bar and the thumbnails do not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...
The Issue: A migrated study that has annotations will display the annotations, but when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.