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. 2,269 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,269 in last 12 months

Showing 4374143760 of 47,970 recalls

FoodJune 4, 2013· ARO Pistachios, Inc.

Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...

The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2013· ARO Pistachios, Inc.

Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...

The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2013· ARO Pistachios, Inc.

Recalled Item: ARO Pistachios Recalled by ARO Pistachios, Inc. Due to Potential Salmonella...

The Issue: Epidemiological evidence in Salmonella Senftenberg outbreak points to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 4, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Cardiovascular Custom Cardiovascular Procedure Kits containing an...

The Issue: Over-Pressure Safety Valves not cleared with an indication for use on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Invacare Corporation

Recalled Item: Invacare Power Wheelchair Recalled by Invacare Corporation Due to Unintended...

The Issue: Unintended slowing or deceleration, and on rare occasion, unanticipated and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Mesa Laboratories, Inc., Bozeman Manufacturing Facility

Recalled Item: Mesa Smart-Read EZTEST BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for...

The Issue: Self-contained steam biological indicator, are recalled because Mesa...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Mesa Laboratories, Inc., Bozeman Manufacturing Facility

Recalled Item: Mesa EZtest BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for use in...

The Issue: Mesa EZTest , Self-contained steam biological indicator, are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Baxa Corporation

Recalled Item: ExactaMix 1200 and 2400 Compounders. Used as an automated pumping Recalled...

The Issue: Baxter Healthcare is recalling certain ExactaMix automated compounding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Respironics California Inc

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California Inc Due to...

The Issue: Respironics California, Inc. has initiated a recall on the V60 ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 4, 2013· Utah Medical Products, Inc

Recalled Item: Deltran Disposable Pressure Transducer Kit (DPT Kit) Extracorporeal...

The Issue: Utah Medical Products, Inc. is recalling certain Deltran Disposable Pressure...

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

Class II — Potential Health HazardOngoing
DrugJune 3, 2013· Actavis

Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 3, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX Evolution System Recalled by Carestream Health Inc. Due to...

The Issue: Due to potential for an x-ray exposure technique change.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2013· Beckman Coulter Inc.

Recalled Item: AU5800 Clinical Chemistry Analyzer with Automation Ready Connection (All...

The Issue: The recall was initiated because Beckman Coulter has identified a software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty Cycler Set Single Conn./Ext DL Product Number: 050-87216...

The Issue: Cassette may leak during set up or during peritoneal dialysis treatment

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Intrathecal Catheter Recalled by Medtronic Neuromodulation Due to...

The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Sutureless Pump Connector Revision Kit Recalled by Medtronic...

The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Intrathecal Catheter Pump Segment Revision Kit Recalled by...

The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed EL Programmable pumps Recalled by Medtronic...

The Issue: Medtronic is providing Healthcare Professionals with important safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic is providing Healthcare Professionals with important safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic INDURA 1P Intrathecal Catheter Recalled by Medtronic...

The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...

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

Class I — Serious Health HazardOngoing