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 2218122200 of 27,456 recalls

Medical DeviceDecember 18, 2014· Spinal Elements, Inc

Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...

The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...

The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...

The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Aesculap, Inc.

Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...

The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2014· Leica Microsystems, Inc.

Recalled Item: Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform...

The Issue: The staining intensity decreases over the shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Trident PSL HA Solid Back 50 mm Includes Dome Hole Recalled by Stryker...

The Issue: Five customer complaints were received for the same batch of Trident PSL...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Synthes, Inc.

Recalled Item: Malleable C- Retractor Recalled by Synthes, Inc. Due to Potential failure...

The Issue: Potential failure and/or corrosion of the internal spring of the retractor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Genetic Testing Institute,inc

Recalled Item: PF4 Concentrated Wash (10x) Recalled by Genetic Testing Institute,inc Due to...

The Issue: Some Lots of PF4 Concentrated Wash (10X) are a slightly more dilute...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· NordicNeuroLab AS

Recalled Item: nordicTumorEx 1.0 nordicTumorEx is an image processing software package to...

The Issue: An error was discovered in the interpretation of certain DICOM header tags...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2014· Biocare Medical Llc

Recalled Item: MUM-1 (Multiple myeloma oncogene-1) Recalled by Biocare Medical Llc Due to...

The Issue: Three lots of MUM-1 may not meet their labeled shelf life, as a drop in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2014· Teleflex, Inc.

Recalled Item: R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal...

The Issue: Teleflex Medical has issued an advisory notification for the RUSCH Curved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2014· Pointe Scientific, Inc.

Recalled Item: Pointe Scientific Creatinine Reagent Catalog number C7539-150 in vitro...

The Issue: Creatinine kit C7539-150 contains Creatinine reagent R1 that is labeled as...

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

Class III — Low RiskOngoing
Medical DeviceDecember 11, 2014· Zimmer, Inc.

Recalled Item: Persona (TASP) Tibial Articular Surface Provisional Shim Recalled by Zimmer,...

The Issue: Potential for delay in surgery and/or ball bearings to be left in the wound....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2014· Owen Mumford USA, Inc.

Recalled Item: Autopen Classic Automatic insulin delivery pen Recalled by Owen Mumford USA,...

The Issue: The dials in the Autopens are not working - the dial does not stay dialed,...

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

Class II — Potential Health HazardOngoing