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. 2,544 recalls have been distributed to Oregon in the last 12 months.
Showing 19761–19780 of 50,914 recalls
Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Recalled...
The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 4MM(H) Recalled...
The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 6MM(H)...
The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion Assembly Pump Guts Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Roller Pump Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion Assembly Pump Guts Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Roller Pump Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...
The Issue: The products are being recalled due to reports of breakage broke at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...
The Issue: The products are being recalled due to reports of breakage broke at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage:...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to A software...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.