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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,363 in last 12 months

Showing 2384123860 of 27,456 recalls

Medical DeviceFebruary 10, 2014· Biomerieux Inc

Recalled Item: bioMerieux PREVI Isola System (General purpose Recalled by Biomerieux Inc...

The Issue: The firm has determined the product may fail to dispense the sample to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2014· Thermedx LLC

Recalled Item: The Thermedx Fluid Management System is designed to provide irrigation...

The Issue: A vendor changed the manufacturing process of a component used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2014· Heraeus Kulzer, LLC.

Recalled Item: BencoDental tartar & stain remover ultrasonic cleaning solution Product...

The Issue: As the result of a complaint to Heraeus Kulzer's customer service...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Infinia and Infinia Hawkeye Nuclear Medicine Systems. For...

The Issue: Potential safety issue related to unintended radial detector motion, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· Baxter Healthcare Corp.

Recalled Item: SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product...

The Issue: Baxter Healthcare Corporation has issued an Urgent Device Correction for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2014· Pega Medical Inc.

Recalled Item: Pega Medical Inc. Recalled by Pega Medical Inc. Due to The Male Components...

The Issue: The Male Components in this lot are made of material with lower strength...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...

The Issue: Potential safety issue related to unintended radial detector motion, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· Djo Surgical

Recalled Item: FMP X-alt Acetabular Liner This acetabular liner is intended for Recalled by...

The Issue: Packaging error -- two different types and sizes of acetabular liners used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· GE Healthcare, LLC

Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to Potential safety...

The Issue: Potential safety issue related to unintended radial detector motion, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· Draeger Medical Systems, Inc.

Recalled Item: Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Recalled by...

The Issue: The battery capacity of the optional PS500 Power Supply Unit of the Infinity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis Systems Product usage: Artis zee is a family Recalled by Siemens...

The Issue: Certain units of the AXIOM Artis Systems are using a flat detector cooling...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...

The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2014· Medtronic Vascular

Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...

The Issue: Incorrect master label.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceFebruary 5, 2014· Synthes, Inc.

Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...

The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...

The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Fisher Scientific Co

Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...

The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F180NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing