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. 2,460 recalls have been distributed to Mississippi in the last 12 months.
Showing 26981–27000 of 49,744 recalls
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...
The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sundream 12 V tanning bed Recalled by ProSun International, LLC Due to The...
The Issue: The 30 minute maximum tanning time has been reduced to 20 minutes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...
The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating IV Pole Rotating IV Pole falls under the category Recalled by...
The Issue: There is the potential for the Rotating IV Pole to fall. A fall could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...
The Issue: The firm made multiple changes to the product requiring the submission of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bull Capsules Recalled by BYL Solutions Inc. Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from Morphine...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from Fentanyl...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLUE PEARL capsules Recalled by Blue Fusion Natural Due to Undeclared Sildenafil
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by Prinston Pharmaceutical Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: confirmed customer complaint of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.