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 2006120080 of 28,488 recalls

Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...

The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...

The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: ONLINE TDM Vancomycin 100 tests Recalled by Roche Diagnostics Operations,...

The Issue: Roche Diagnostics Operations, Inc. has issued a voluntary recall for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Recalled by Philips Medical Systems (Cleveland)...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Physio-Control, Inc.

Recalled Item: LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External...

The Issue: LIFEPAK CR Plus Automated External Defibrillators (AED) or LIFEPAK EXPRESS...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access software. The firm name on the label is Merge Healthcare...

The Issue: Software displayed incorrect prior reports in the viewport area, only when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Upgrade Model 882454 Recalled by Philips Medical Systems...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to The...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Crit Line in a Clip (CLiC). CliC P/N: CL 10041001 Recalled by Fresenius...

The Issue: Use of the Blood Pressure Graph located on the Crit-Line screen of the 2008T...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 29 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics started receiving customer complaints for biased...

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

Class III — Low RiskOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Left Foot/20mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Baxter Healthcare Corp.

Recalled Item: PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy...

The Issue: Presence of leaks near top of the PrismaSate bags

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Right Foot/20mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing