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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 2722127240 of 27,456 recalls

Medical DeviceSeptember 8, 2011· Abbott Point Of Care Inc.

Recalled Item: Fuso Analyzer 300F Recalled by Abbott Point Of Care Inc. Due to Some i-Stat...

The Issue: Some i-Stat Analyzers become uncomfortably hot to touch in the are of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2011· Exactech, Inc.

Recalled Item: OPTETRAK LOGIC TIBIAL INSERT POSTERIOR STABILIZED***Match Component Colors 6...

The Issue: Exactech, Inc. of Gainesville, FL is recalling their Optetrak Logic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2011· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage:...

The Issue: In GUI inquiry, searching by ID (CID) may return the wrong patient...

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

Class III — Low RiskOngoing
Medical DeviceAugust 12, 2011· Linvatec Corp. dba ConMed Linvatec

Recalled Item: CrossFT Punch Recalled by Linvatec Corp. dba ConMed Linvatec Due to ConMed...

The Issue: ConMed Linvatec recalled lot number #156920, PFT-45M, CrossFT Punch because...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2011· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza image processing system image processing radiological...

The Issue: The firm became aware of an unintended behavior when using the syngo.plaza....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxC 880i Recalled by Beckman Coulter Inc. Due to The recall was...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2011· Beckman Coulter Inc.

Recalled Item: UniCel Dxl 600 Access Immunoassay System Recalled by Beckman Coulter Inc....

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2011· Beckman Coulter Inc.

Recalled Item: UniCel Dxl 800 Access Immunoassay System Recalled by Beckman Coulter Inc....

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2011· Beckman Coulter Inc.

Recalled Item: Access Immunoassay Systems Total T4 Calibrators Recalled by Beckman Coulter...

The Issue: A recall communication was initiated because Beckman has identified that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2011· GE Healthcare, LLC

Recalled Item: GE Recalled by GE Healthcare, LLC Due to Fastener bolts on the heat...

The Issue: Fastener bolts on the heat exchanger were not properly torqued and part of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2011· Discus Dental LLC

Recalled Item: SL3 SOFT-TISSUE Laser (Model LR2002) Recalled by Discus Dental LLC Due to...

The Issue: The firm is initiating this recall of the SL3 Soft Tissue Laser equipped...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2011· GE Healthcare, LLC

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

The Issue: GE Healthcare has recently become aware of an issue associated with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2011· First Medical Source LLC

Recalled Item: Medpro Elastomeric Infusion Pump. AccuFlux Recalled by First Medical Source...

The Issue: Please be aware that this is not a new recall. The firm has taken action;...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2011· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model...

The Issue: Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set stability claim...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2011· Baxter Healthcare Corporation

Recalled Item: Sigma Spectrum VOLUMETRIC INFUSION PUMP Recalled by Baxter Healthcare...

The Issue: Recall expansion; the infusion pumps have the potential to fail causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 5, 2011· Keystone Dental Inc

Recalled Item: Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: Recalled by...

The Issue: Mislabeled: Genesis Straight Esthetic 5.0mm Contour ,3mm cuff labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2011· Keystone Dental Inc

Recalled Item: Genesis Straight Esthetic 5.0 mm 3. mm Cuff Abutment Part Recalled by...

The Issue: Mislabeled: Genesis Straight Esthetic 4.0mm Contour ,1mm cuff labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2011· Linvatec Corp. dba ConMed Linvatec

Recalled Item: Catheter Irrigation Set labeled in part: ***24K Arthroscopy Outflow/Suction...

The Issue: ConMed Linvatec recalled their 24k Arthroscopy Outflow/Suction Tubing Set...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2011· Epocal Inc

Recalled Item: epoc Blood Analysis BGEM Test Cards for use with the Recalled by Epocal Inc...

The Issue: Customer reported problem while performing incoming QC of newly received lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2011· The Anspach Effort, Inc.

Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...

The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.

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

Class II — Potential Health HazardOngoing