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 3244132460 of 50,914 recalls

Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED OVERSIZED...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Alere San Diego, Inc.

Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...

The Issue: Encoded with incorrect ranges that are not consistent with the ranges...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Baxter Healthcare Corp.

Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...

The Issue: Potential presence of particulate matter on the blood side of the dialyzer

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

Class II — Potential Health HazardOngoing
FoodOctober 11, 2016· JJBL LLC

Recalled Item: The Most Awesome Chocolate Bar Ever Recalled by JJBL LLC Due to Undeclared Wheat

The Issue: The Most Awesome Chocolate Bar Ever is recalled due to undeclared wheat.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 11, 2016· Roland Foods, LLC.

Recalled Item: Roland¿ Preserved Lemons Recalled by Roland Foods, LLC. Due to Undeclared...

The Issue: The product contains undeclared sulfites based on sampling and analysis by...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 11, 2016· JJBL LLC

Recalled Item: The Stone Ground Peanut Butter Chocolate Bar Recalled by JJBL LLC Due to...

The Issue: The Stone Ground Peanut Butter Chocolate Bar is recalled due to undeclared...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 11, 2016· Nuvectra

Recalled Item: Algovita Spinal Cord Stimulation System Recalled by Nuvectra Due to Nuvectra...

The Issue: Nuvectra is conducting a recall due to two clinical risks that are...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...

The Issue: An error may occur with the display of dose computed on images other than...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· Abbott Laboratories

Recalled Item: ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay Recalled by...

The Issue: Abbott has identified negative interference from the drug N-Acetyl Cysteine...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF MultiGen¿ Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker Instruments is voluntarily recalling the Care...

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

Class III — Low RiskOngoing
FoodOctober 10, 2016· Rosa Foods HQ

Recalled Item: Soylent Food Bars Recalled by Rosa Foods HQ Due to Rosa Foods is recalling...

The Issue: Rosa Foods is recalling Soylent Bar because a number of their customers have...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to St Jude Medical is recalling...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Fortify VR Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Calibrator For in vitro diagnostic use in the Recalled by...

The Issue: Siemens has confirmed that the DBIL_2 Assigned Calibrator Values (ACV)...

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

Class II — Potential Health HazardOngoing
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets Recalled by Boehringer Ingelheim...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Rotating Adult Craniotome Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing