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 2692126940 of 28,488 recalls

Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) IRON Calibrator (DC85) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints of IRON calibrations...

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

Class III — Low RiskOngoing
Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An...

The Issue: The analytical sensitivity claim of 6 ug/dL (1.1 umol/L) in the Instructions...

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

Class III — Low RiskOngoing
Medical DeviceDecember 19, 2012· Elekta, Inc.

Recalled Item: Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1...

The Issue: The DICOM tags do not contain sufficient information for XVI to identify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Hamilton Medical Inc

Recalled Item: HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON...

The Issue: Analysis of a customer complaint has shown that during ventilation of small...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R)...

The Issue: Siemens has confirmed an increase on absorbance errors when calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For...

The Issue: The microelectrodes are not flush with the silastic substrate, may contain...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Abbott Laboratories, Inc

Recalled Item: ARCHITECT HBsAg Qualitative Assay Recalled by Abbott Laboratories, Inc Due...

The Issue: Abbott has identified that assay files for the ARCHITECT HBsAg Qualitative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing