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. 2,470 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,470 in last 12 months

Showing 2638126400 of 50,914 recalls

Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2018· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: This email is to provide notification that, due to a software bug that has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2018· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Recalled by Steris...

The Issue: The firm has become aware that the Reliance 1227 Cart and Utensil...

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

Class II — Potential Health HazardOngoing
FoodMay 23, 2018· New Seasons Market LLC

Recalled Item: Blueberry Buckwheat Muffin Recalled by New Seasons Market LLC Due to...

The Issue: Blueberry Buckwheat Muffin is recalled because the Contains statement does...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 23, 2018· New Seasons Market LLC

Recalled Item: Honey Oat Bran Muffin Recalled by New Seasons Market LLC Due to Honey Oat...

The Issue: Honey Oat Bran Muffin is recalled because the Contains statement does not...

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

Class III — Low RiskOngoing
Refund
FoodMay 23, 2018· New Seasons Market LLC

Recalled Item: Meyer Lemon Chia Muffin Recalled by New Seasons Market LLC Due to Meyer...

The Issue: Meyer Lemon Chia Muffin is recalled because the Contains statement does not...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 23, 2018· New Seasons Market LLC

Recalled Item: Mini Chocolate Croissants Recalled by New Seasons Market LLC Due to Mini...

The Issue: Mini Chocolate Croissants are recalled because the Ingredients statement and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2018· Divvies LLC

Recalled Item: simply delicious Divvies SEMI-SWEET PEPPERMINT BARS made to share CHOCOLATE...

The Issue: Product may contain traces of milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 23, 2018· New Seasons Market LLC

Recalled Item: Vegan Chocolate Almond Muffin Recalled by New Seasons Market LLC Due to...

The Issue: Vegan Chocolate Almond Muffin is recalled because the Contains statement...

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

Class III — Low RiskOngoing
Refund
FoodMay 23, 2018· New Seasons Market LLC

Recalled Item: Mini Butter Croissants Recalled by New Seasons Market LLC Due to Mini Butter...

The Issue: Mini Butter Croissants are recalled because the Ingredients statement and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 22, 2018· Lake Michigan Distilling Co LLC

Recalled Item: Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol Recalled by Lake...

The Issue: Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: Large QWIX Recalled by NewDeal SA Due to Use of the impacted product may...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: UNI-CP Recalled by NewDeal SA Due to Use of the impacted product may cause a...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing