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. 2,457 recalls have been distributed to Rhode Island in the last 12 months.
Showing 14001–14020 of 27,456 recalls
Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...
The Issue: There is a potential for an incorrect dose distribution calculation by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades:Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Blades Monopolar Recalled by Gyrus ACMI, Inc. Due to Olympus...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Malleable Recalled by Gyrus ACMI, Inc. Due to Olympus Diego...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Diego Elite Console MDCONS 100 Recalled by Gyrus ACMI, Inc. Due to...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There were multiple issues identified in the system software which required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime Recalled by Siemens Healthcare Diagnostics,...
The Issue: There were multiple issues identified in the system software which required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There were multiple issues identified in the system software which required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...
The Issue: Elevated rates of false positive results for Campylobacter and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...
The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.