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. 2,499 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,499 in last 12 months

Showing 2170121720 of 28,488 recalls

Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 3.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2015· Abbott Laboratories, Inc

Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...

The Issue: Incorrect tubing.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2015· Intuitive Surgical, Inc.

Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...

The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· DePuy Orthopaedics, Inc.

Recalled Item: Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120)...

The Issue: DePuy Orthopaedics, Inc. is initiating a voluntary recall of select lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...

The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...

The Issue: Complaints that the femoral head could not be assembled with its...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Stryker Spine

Recalled Item: Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled by...

The Issue: The Inserter Inner Shaft would not fit through the Inserter. The inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Biocare Medical, LLC

Recalled Item: Smooth Muscle Action (SMA) Immunohistochemistry reagent. Catalog numbers:...

The Issue: Certain catalog numbers and lots of Smooth Muscle Actin may stain some cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-Ray System Recalled by...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Brilliance iCT Computed Tomography X-Ray System Recalled...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-Ray System Recalled...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Ingenuity Elite Computed Tomography X-Ray System Recalled...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-Ray System Recalled...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2015· Philips Healthcare

Recalled Item: Philips Healthcare Brilliance iCT SP Computed Tomography X-Ray System...

The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2015· Dako North America Inc.

Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...

The Issue: There is a defect in one lot of a buffer, non-specific background staining...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2015· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: -Pipeline Embolization Device -Pipeline Flex Embolization Device The...

The Issue: The firm is recalling Pipeline and Pipeline Flex Embolization Devices from...

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

Class II — Potential Health HazardOngoing