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. 2,558 recalls have been distributed to Mississippi in the last 12 months.
Showing 16881–16900 of 49,744 recalls
Recalled Item: Tucson Tamale Blue Corn Recalled by Tucson Tamale Wholesale Company, LLC Due...
The Issue: Plastic pieces (1-2 cm) were discovered inside cans of tomatoes which were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CareLink Personal Software Therapy Management Software Tool for Diabetes...
The Issue: Incomplete basal rate information may be transmitted leading to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...
The Issue: A710 Intellis Clinician Application has a software issue that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Tip Guide- indicated for use in open Recalled by ConMed...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Elbow Guide-indicated for use in open and Recalled by...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling
The Issue: The product is mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilation System Recalled by Hill-Rom Manufacturing, Inc. Due to...
The Issue: Under certain conditions, there is a risk for fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levocetirizine Dihydrochloride Tablets Recalled by InvaTech Pharma...
The Issue: Failed Impurities/Degradation Specifications: One lot of Levocetirizine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA Due to Superpotent...
The Issue: Superpotent Drug: High out-of-specification assay results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Canon PET-CT SCANNER Recalled by Canon Medical System, USA, INC. Due to A...
The Issue: A software problem has been identified which could result in the diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Adult Elongated O2/CO2 Mask - Product Usage: intended Recalled by Westmed,...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Elongated CO2/O2 Mask Recalled by Westmed, Inc. Due to There is a...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK Recalled by...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Capiox FX25 (West) Advance Oxygenator- with left port Recalled by Terumo...
The Issue: Capiox FX25 Advance oxygenator may be the incorrect configuration (East vs....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4 Recalled by RAYSEARCH LABORATORIES AB Due to Two issues were...
The Issue: Two issues were found with the treatment plan report: 1) There may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: Recalled by...
The Issue: Revised Instruction Manual to the most accurate illustration for Mayfield...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.