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. 2,401 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,401 in last 12 months

Showing 1838118400 of 27,456 recalls

Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2016· 3M Company - Health Care Business

Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...

The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...

The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 25, 2016· Trumpf Medical Systems, Inc.

Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...

The Issue: Trumpf has identified six incidents of pinched cables.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...

The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...

The Issue: Disengaged screw head could potentially not be retained in the Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...

The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Domain Surgical, Inc.

Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...

The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Beckman Coulter Inc.

Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Beckman Coulter Inc.

Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Recovery of Incorrect Isocenter -operational change

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2016· Centurion Medical Products Corporation

Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...

The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...

The Issue: A product issues happens for RF projection images. If user measures on RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens is providing software update version VA50A_SP3 to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Software defect:2D projection of contours in Verity. The defect causes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Ekla Corporation

Recalled Item: NOVAPLUS(R) Pregnancy Cassette Device with Droppers Recalled by Ekla...

The Issue: Incorrect hCG results

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Beckman Coulter Inc.

Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile...

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Sterile Disposable Probes sold individually Recalled by Ultroid...

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

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

Class II — Potential Health HazardOngoing