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. 2,457 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,457 in last 12 months

Showing 2712127140 of 28,488 recalls

Medical DeviceNovember 5, 2012· Medrad Inc

Recalled Item: MEDRAD Hand Controller Sheath Recalled by Medrad Inc Due to The seal between...

The Issue: The seal between the white polyethylene and the clear plastic may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Brookstone Company, Inc.

Recalled Item: Brookstone Heated Body Bean Recalled by Brookstone Company, Inc. Due to...

The Issue: Additional Warning Statement to prevent burns to the skin

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Del Mar Reynolds Medical, Ltd.

Recalled Item: BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are...

The Issue: The BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Trauma Nail System. The devices are indication for bone fixation....

The Issue: Recall was initiated due to the possibility that the outer pouch was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B...

The Issue: Ortho Clinical Diagnostics is recalling certain lots of the Vitros Anti-HBs...

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

Class III — Low RiskOngoing
Medical DeviceNovember 1, 2012· Merge Healthcare, Inc.

Recalled Item: CADstream software. Product Usage: CADstream is an image processing system...

The Issue: An incorrect biopsy or missed target could result if the incorrect grid is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Biomet, Inc.

Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 8.0 THRU 12.5 Recalled by Biomet, Inc....

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Beckman Coulter Inc.

Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to It has...

The Issue: It has been determined that, in some cases, pulley drive components have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Operations,...

The Issue: On cobas c 701 and cobas c 702 modules of the Cobas 8000 series analyzer, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Biomet, Inc.

Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 13.0 thru 20.0 Recalled by Biomet, Inc....

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing