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. 2,681 recalls have been distributed to Oregon in the last 12 months.
Showing 1121–1140 of 28,488 recalls
Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...
The Issue: Potential for activation of an abnormal alarm pause.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...
The Issue: Potential for barb non-engagement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Radiology Solutions software version 14.2.2 Recalled by...
The Issue: Due to software issue, radiology reports may not be fully displayed when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT Recalled by...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. IQon Spectral CT Recalled by...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.