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 2042120440 of 50,914 recalls

FoodNovember 4, 2019· Whole Foods Market

Recalled Item: SALAD BROCCOLI KALE served on the hot bar Recalled by Whole Foods Market Due...

The Issue: Possible contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2019· Whole Foods Market

Recalled Item: Salmon Dinner with Lemon Herb for 2 packaged in the store Recalled by Whole...

The Issue: Possible contamination with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2019· Whole Foods Market

Recalled Item: Wedge Charred Corn Salad served on the salad bar Recalled by Whole Foods...

The Issue: Possible contamination with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2019· Whole Foods Market

Recalled Item: SLAW CARROT GINGER served on the hot bar Recalled by Whole Foods Market Due...

The Issue: Possible contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2019· Whole Foods Market

Recalled Item: Single meal Chicken Rosemary Paleo sold in the chef's case Recalled by Whole...

The Issue: Possible contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2019· Whole Foods Market

Recalled Item: Slaw Recalled by Whole Foods Market Due to Potential Listeria Contamination

The Issue: Possible contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2019· Whole Foods Market

Recalled Item: Chicken Orange Sesame sold on the hot bar Recalled by Whole Foods Market Due...

The Issue: Possible contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2019· Renaissance Food Group, LLC

Recalled Item: Kroger Mushroom Stir Fry Blend 10 oz. Recalled by Renaissance Food Group,...

The Issue: Potential Listeria monocytogenes contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2019· Renaissance Food Group, LLC

Recalled Item: Kroger Stir Fry Blend 16 oz. Recalled by Renaissance Food Group, LLC Due to...

The Issue: Potential Listeria monocytogenes contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 4, 2019· Shimadzu Medical Systems

Recalled Item: Trinias DAP Meter Recalled by Shimadzu Medical Systems Due to The DAP meters...

The Issue: The DAP meters were found to be outside of tolerance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Immunodiffusion (ID) Antigen Recalled by Immuno-Mycologics, Inc...

The Issue: False positive results due to potential contamination of reagent.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Medacta Usa Inc

Recalled Item: Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS Recalled by Medacta...

The Issue: Certain lot numbers of the Medacta Humeral Anatomical Cementless Metaphysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Integra Lifesciences Sales Llc

Recalled Item: Ascension¿ Silicone PIP-Silicone PIP Sz 1 Recalled by Integra Lifesciences...

The Issue: Silicone PIP Implant mislabeled as a size 1 implant on the outer packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Healix Knotless ADV BR 4.75 Suture Anchor Recalled by DePuy Mitek, Inc., a...

The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Healix Knotless ADV BR 5.5 Suture Anchor Recalled by DePuy Mitek, Inc., a...

The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Becton Dickinson & Company

Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...

The Issue: The indicator may show available charge when the battery is close to...

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

Class II — Potential Health HazardOngoing