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. 2,438 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,438 in last 12 months

Showing 3600136020 of 50,914 recalls

Medical DeviceJanuary 7, 2016· Wfr/aquaplast Corp

Recalled Item: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Recalled...

The Issue: Some of the Access ClearVue Prone Breast devices may contain scales that are...

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

Class II — Potential Health HazardOngoing
FoodJanuary 7, 2016· Madison One Acme Inc

Recalled Item: Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills Recalled by...

The Issue: Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 6, 2016· Bearded Brothers LLC

Recalled Item: Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g . Recalled by...

The Issue: Mold on energy bars.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 6, 2016· Bearded Brothers LLC

Recalled Item: Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g . Recalled by Bearded...

The Issue: Mold on energy bars.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Pressure Monitoring Sets and Trays The subject sets Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing