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. 2,359 recalls have been distributed to Mississippi in the last 12 months.
Showing 46921–46940 of 49,744 recalls
Recalled Item: Plum A+ Infusion Pump. List Number 11971. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump. List Number 11973. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump System. List Number 12348. The Plum Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heritage Labs Path Study Extra Supplies Kit Recalled by Heritage Labs...
The Issue: The product has a Lithium Heparin contaminant which could adversely affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to In rare...
The Issue: In rare instances, the BCI¿ Remote Alarm Cables (BCI¿ Cable) are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: Observed instability of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineNet Anterior Cervical Cage Recalled by SpineNet Due to The recall...
The Issue: The recall decision has been made because because it has recently been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialist 2 IM Rod Recalled by DePuy Orthopaedics, Inc. Due to Potential...
The Issue: Potential for the IM rod to break, leaving fragments in the patient....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended Release Tablets Recalled by American Health...
The Issue: Failed Stability Specifications; out of specification results at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benjamins Infants Gripe Mixture Recalled by Carib Import & Export, Inc. Due...
The Issue: CGMP Deviations: this product is being recalled because an FDA inspection...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SourceCF(R) Pediatric Drops Recalled by Aptalis Pharma Us Inc Due to The...
The Issue: The data suggests that the formulation does not support the shelf life of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.