Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,351 recalls have been distributed to Rhode Island in the last 12 months.
Showing 25741–25760 of 27,456 recalls
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: 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: 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 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. 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. 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+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+ 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 12618. 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+ Hyperbaric Infusion Pump. List Number 11005. 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: 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: 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: 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: 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: Gen-Probe LIFECODES PF4 Enhanced assay Recalled by Genetic Testing...
The Issue: Lifecodes PF4 Enhanced assay, lot number 3000389, is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and...
The Issue: EsophyX2Plus device was not validated under actual or simulated use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.