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 2280122820 of 27,456 recalls

Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit Recalled by...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology and PASV Valve Technology Maximal...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2014· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) SafeLiner Suction Canister Kit Recalled by DeRoyal Industries Inc...

The Issue: These lots of suction canisters and lids have an insufficient seal under low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2014· DeRoyal Industries Inc

Recalled Item: Suction canisters labels as follows: 1) DeRoyal(R) SUCTION CANISTER Recalled...

The Issue: These lots of suction canisters and lids have an insufficient seal under low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Beckman Coulter Inc.

Recalled Item: UniCel 600/800 Access Immunoassay Systems are in vitro diagnostic devices...

The Issue: Beckman Coulter is recalling the Sample Probe Cable because nonconforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Maquet Medical Systems USA

Recalled Item: TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Recalled by...

The Issue: The wrong movement results on the MAGNUS OR table. The button commands on...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia Recalled by Philips Medical Systems, Inc. Due to When a fused series...

The Issue: When a fused series of a sagittal, coronal or radial multi station scan is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT (Phenytoin) Slides Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics identified a potential for biased results to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Ellipse Implantable Cardioverter Defibrillators (ICDs) Recalled by St Jude...

The Issue: An anomaly may result in delayed, partial, or no delivery of high voltage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: 83" (211 cm) Appx 10.3 mL Recalled by ICU Medical, Inc. Due to ICU is...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Appx 12.3 ml Recalled by ICU Medical, Inc. Due to ICU is...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens CentraLink Data Management System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has identified a task scheduler issue with...

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

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

Recalled Item: Monaco The Monaco system is used to make treatment plans Recalled by Elekta,...

The Issue: Incorrect Delivery of Composite VMAT Fields - When DICOM is exporting an arc...

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

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

Recalled Item: 4D Integrated Treatment Console (4DITC) Recalled by Varian Medical Systems,...

The Issue: Due to user error, the 4DITC can improperly allow users to clear a safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista¿ CHEM 1 CAL Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints for low recovery of...

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

Class II — Potential Health HazardOngoing