Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,475 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,475 in last 12 months

Showing 2290122920 of 28,488 recalls

Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...

The Issue: Incorrect size printed on the Milex Pessary Kit packaging label

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...

The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...

The Issue: Possibility of image artifacts during data acquisition when using Adaptive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...

The Issue: Philips discovered that a software defect exists in marketed product wherein...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Arrow International Inc

Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...

The Issue: Outer package product label incorrectly identifies the product as FiberOptix...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Derma Pen, LLC

Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...

The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse...

The Issue: Under certain circumstances the patient Demographics in a report exported...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: FujiMedical Synapse Cardiovascular I ProSolv CardioVascular. A picture...

The Issue: Measurement values in the EMR may not accurately the actual measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Norwex Usa Inc

Recalled Item: Manual Toothbrush Recalled by Norwex Usa Inc Due to The toothbrush head can...

The Issue: The toothbrush head can potentially disengage from the handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Synthes, Inc.

Recalled Item: Synthes Inserter for Titanium Elastic Nails Recalled by Synthes, Inc. Due to...

The Issue: The Inserter has the potential for mechanical failures such as breakage of...

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

Class II — Potential Health HazardOngoing