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. 2,511 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,511 in last 12 months

Showing 2084120860 of 50,914 recalls

FoodOctober 1, 2019· E.A. Sween Co.

Recalled Item: Market Sandwich Artisan Style Ranch Chicken Salad sandwich Recalled by E.A....

The Issue: Various sandwiches have the potential to be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 1, 2019· E.A. Sween Co.

Recalled Item: Market Sandwich Dill Egg Salad on Classic White Bread Recalled by E.A. Sween...

The Issue: Various sandwiches have the potential to be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 1, 2019· E.A. Sween Co.

Recalled Item: Tuna Salad on Wheat Bread Recalled by E.A. Sween Co. Due to Potential...

The Issue: Various sandwiches have the potential to be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 1, 2019· E.A. Sween Co.

Recalled Item: Deli Express Egg Salad on Homestyle White Bread Recalled by E.A. Sween Co....

The Issue: Various sandwiches have the potential to be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 1, 2019· E.A. Sween Co.

Recalled Item: Market Sandwich Everything Bagel with Smoked Ham Recalled by E.A. Sween Co....

The Issue: Various sandwiches have the potential to be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
FoodSeptember 30, 2019· Jumbo Foods, Inc.

Recalled Item: Wedge Chicken Salad Recalled by Jumbo Foods, Inc. Due to Potential Listeria...

The Issue: Product is recalled due to a potential for contamination with Listeria...

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

Class I — Serious Health HazardOngoing
Refund