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 2400124020 of 27,456 recalls

Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Recalled by...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100S Sterilization System Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Covidien

Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...

The Issue: Covidien is conducting a voluntary field corrective action on Puritan...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee Ceiling Systems. Angiographic x-ray system. Recalled by...

The Issue: During the lifetime of Artis zee Ceiling systems, there is an increased wear...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...

The Issue: Ensuring all customers have the tools to assist in verifying the setting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: Sterility of medical devices intended for use in surgical procedures may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· King Systems Corp.

Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...

The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· BioHorizons Implant Systems Inc

Recalled Item: External Implant RBT Recalled by BioHorizons Implant Systems Inc Due to The...

The Issue: The body length of the External Implant 40105D3 Lot 1302762 labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator with CO2/EtCO2 Measurement The...

The Issue: MRx defibrillator displays a -?- for EtCO2 and does not display EtCO2 values...

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

Class II — Potential Health HazardOngoing