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. 2,429 recalls have been distributed to Mississippi in the last 12 months.
Showing 35781–35800 of 49,744 recalls
Recalled Item: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by...
The Issue: The device might fail to detect air in line while infusing the medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...
The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc....
The Issue: Kontos Falafel Mix contains undeclared wheat allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....
The Issue: Chemical Contamination: The product may contain trace amounts of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...
The Issue: Chemical Contamination: The product may contain trace amounts of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...
The Issue: Reporting feature times out after inactivity for more than an hour sending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...
The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Traditional Round Yellow Tortillas. Sold under the brand names of: Better...
The Issue: Firm was notified by a customer that the product contained an undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine HCl 10 mg Tablet Recalled by Perrigo Company PLC Due to Failed...
The Issue: Failed Impurity/Degradations Specifications; impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...
The Issue: The firm is conducting a product correction due to an increase in U90-382 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.