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. 2,448 recalls have been distributed to Mississippi in the last 12 months.
Showing 26441–26460 of 28,172 recalls
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic...
The Issue: Potential failure of the braking system that controls the O-arm Imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus...
The Issue: During the course of product monitoring, Siemens became aware of a tolerance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echelon Recalled by Hitachi Medical Systems America Inc Due to Hitachi...
The Issue: Hitachi discovered a software error that can occur when simultaneously...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Recalled by QIAGEN...
The Issue: CMV RG PCR kits may contain a mixture of incorrect vials among the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Recalled by QIAGEN...
The Issue: CMV RG PCR kits may contain a mixture of incorrect vials among the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring sets with VAMP Plus closed blood sampling system...
The Issue: The device is being recalled because the firm has received multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Vascular...
The Issue: Vascular Solutions, Inc has discovered a potential problem with a number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bacterin Elutia Recalled by Bacterin International, Inc. Due to A portion of...
The Issue: A portion of a silicone wound drain was found to be cracked.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The...
The Issue: Philips HeartStart XL+ Defibrillator/Monitor may become locked out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Eclipse Treatment Planning System for Radiotherapy Recalled by Varian...
The Issue: The calculation of dose dynamic plans containing different energy fields is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.