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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.
Showing 2401–2420 of 27,456 recalls
Recalled Item: DLP Pediatric One-Piece Arterial Cannulae Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Series Angled Tip Arterial Cannula Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist Recalled by Abiomed, Inc. Due to Optical...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP with SmartAssist Recalled by Abiomed, Inc. Due to Optical Sensors...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biological Recalled by HF Acquisition Co LLC Due to Spore test strip...
The Issue: Spore test strip monitoring system, designed for routine monitoring of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nuwellis AquaFlexFlow UF 500 Plus Recalled by Nuwellis Inc Due to The...
The Issue: The AquaFlexFlow UF 500 Plus extracorporeal blood circuit used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic NanoCross Elite PTA catheter Recalled by ev3 Inc Due to There is...
The Issue: There is the potential for in-vivo balloon deflation issues, including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Tee T-Piece Resuscitator Recalled by Mercury Enterprises, Inc. dba...
The Issue: Gas powered emergency resuscitator has a circuit flow controller...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee insert package may contain an acetabular system, which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers:...
The Issue: Potential for two issues: 1. Bent or detached heater wire; 2. Silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model...
The Issue: Potential for two issues: 1. Bent or detached heater wire; 2. Silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Titanium Abutments Recalled by DDS Lab Due to Certain definitive...
The Issue: Certain definitive dental implant restoration cases may have included a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portrait Core Services Recalled by GE Medical Systems, LLC Due to There is a...
The Issue: There is a software issue that can result in the loss of patient monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.