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. 2,486 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,486 in last 12 months

Showing 2368123700 of 50,914 recalls

FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Jin Ramen Mild Bowl Recalled by Ottogi America Inc Due to Undeclared...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Beijing Spicy Seafood Noodle 5PK 1lb 5.16oz x 8pk Recalled by Ottogi...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Jjajang Bokki (Bowl) 4.23oz x 12ea Item #21502157 Manufactured...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Beijing JJajang Noodle 5PK 1lb 7.81oz x 8pk Item Recalled by Ottogi...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Spicy Seafood Flavor Udon Odongtong (Bowl) 3.53oz x 12ea Recalled by...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Snack Ramen 5PK Recalled by Ottogi America Inc Due to Undeclared Allergen

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Yeul Ramen (Bowl) 4.06oz x 12ea Item #21305007 Manufactured Recalled...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Ppushu Ppushu Spicy Flavor 3.17oz x 40ea Item #21503008 Recalled by...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Ppushu Ppushu Bulgogi Flavor 3.17oz x 40ea Item #21503005 Recalled by...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Jin Ramen Spicy Recalled by Ottogi America Inc Due to Undeclared Allergen

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Ramen Bokki (Cup) 4.23oz x 12ea Item #21309009 Manufactured Recalled...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask Recalled by...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit Recalled by Westmed, Inc. Due...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask Recalled by...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Miami Device Solutions, LLC.

Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...

The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2019· Teleflex Medical

Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...

The Issue: The device labels are not UDI compliant. The missing UDI compliance...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 14, 2019· Teleflex Medical

Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...

The Issue: The device labels are not UDI compliant. The missing UDI compliance...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 14, 2019· Arthrex, Inc.

Recalled Item: Arthrex Burr Recalled by Arthrex, Inc. Due to Devices may generate excessive...

The Issue: Devices may generate excessive heat during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2019· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU MobileDaRt Evolution (MX8 Version) Recalled by Shimadzu Medical...

The Issue: In these units, the brake is usually released by gripping the drive handle...

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

Class II — Potential Health HazardOngoing