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. 2,368 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,368 in last 12 months

Showing 2282122840 of 27,456 recalls

Medical DeviceAugust 18, 2014· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon Oval MRI system is a diagnostic imaging device Recalled by...

The Issue: The Gradient Coil was found to have a failure mode that allowed it to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Elekta, Inc.

Recalled Item: FOCAL Sim Workstation Recalled by Elekta, Inc. Due to When DICOM is...

The Issue: When DICOM is exporting an arc plan (VMAT, Dynamic Conformal of 3D Static...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Data Innovations, LLC

Recalled Item: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below...

The Issue: Potential issues with the ProVue driver have been identified which may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Lumenis, Inc.

Recalled Item: Array LaserLink Recalled by Lumenis, Inc. Due to Lumenis initiated a...

The Issue: Lumenis initiated a field-correction for the Array Laser Link",...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp....

The Issue: The peel strength of the inner blister may have been below internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics RESTORATION Acetabular Augment System Recalled...

The Issue: The peel strength of the inner blister may have been below internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp....

The Issue: The peel strength of the inner blister may have been below internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· The Anspach Effort, Inc.

Recalled Item: Synthes Small Electric Drive (SED). For use in general traumatology....

The Issue: The affected Small Electric Drive (SED) may operate solely in reverse mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ HbA1c Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· Sam Medical Products

Recalled Item: SAM Junctional Tourniquet (SJT) Auxiliary Recalled by Sam Medical Products...

The Issue: SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur XP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Biofire Defense

Recalled Item: JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is...

The Issue: BioFire Defense, LLC is initiating a field action for JBAIDS Software...

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: V5Ms Transesophageal transducers Recalled by Siemens Medical Solutions USA,...

The Issue: Reports of deterioration of material covering the articulating section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Maquet Cardiovascular, LLC

Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...

The Issue: An internal finding identified the presence of pinholes/cuts in some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Volcano Corporation

Recalled Item: Volcano TrakBack II Disposable Pullback Device Recalled by Volcano...

The Issue: Internal testing had identified a potential breach to the sterile barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur Immunoassay System Recalled by Siemens Healthcare Diagnostics...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...

The Issue: Water may leak into the center gas lumen of the Patient Circuit

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

Class II — Potential Health HazardOngoing