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. 2,368 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,368 in last 12 months

Showing 4416144180 of 50,914 recalls

FoodJanuary 21, 2014· Tijuana'S Produce Co.

Recalled Item: Cactus Leaves (Nopales) Recalled by Tijuana'S Produce Co. Due to Tijuana's...

The Issue: Tijuana's Produce is recalling cactus leaves (nopales) due to unapproved...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 21, 2014· Golden Technologies, Inc.

Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...

The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Dako North America Inc.

Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...

The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...

The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless...

The Issue: GE Healthcare has recently become aware of a software issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Edwards Lifesciences, LLC

Recalled Item: Crimper Model 9100CR26 The Crimper is indicated for use in Recalled by...

The Issue: Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2014· Medical Information Technology, Inc.

Recalled Item: MEDITECH Microbiology - Calculator/data processing module Recalled by...

The Issue: Potential for patient results being removed from LAB/EMR.

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2014· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Foreign Tablets: A product complaint was received by a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Cooling Eye Drops Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Dry Eye Recalled by The Mentholatum Co. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2014· DeRoyal Industries Inc

Recalled Item: DeRoyal ST. Circumcision Clamp Recalled by DeRoyal Industries Inc Due to...

The Issue: Three lots of circumcision clamps were manufactured out of specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2014· CareFusion 303, Inc.

Recalled Item: Trifurcated Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...

The Issue: CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products 25-OH Vitamin D Total Calibrators Recalled...

The Issue: Ortho Clinical Diagnostics has determined that the VITROS Immunodiagnostic...

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

Class III — Low RiskOngoing
DrugJanuary 14, 2014· Traxx International Corp

Recalled Item: Guaifenesin USP Recalled by Traxx International Corp Due to Presence of...

The Issue: Presence of Foreign Matter: Guaifenesin API powder is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Subpotent Drug: Assay results obtained during stability testing for...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 14, 2014· Paskesz Candy Co.,Inc.

Recalled Item: PASKESZ PREMIUM BELGIAN CHOCOLATE Recalled by Paskesz Candy Co.,Inc. Due to...

The Issue: Paskesz Candy Co., Inc. has recalled PREMIUM BELGIAN CHOCOLATE coins due to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 14, 2014· Instrumentarium Dental, PaloDEx Group Oy

Recalled Item: The FOCUS is a microprocessor controlled intra-oral x-ray unit with Recalled...

The Issue: Instrumentarium Dental has delivered a number of FOCUS 3.0 Intraoral X-ray...

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

Class II — Potential Health HazardOngoing