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. 2,646 recalls have been distributed to Oregon in the last 12 months.
Showing 6621–6640 of 50,914 recalls
Recalled Item: SCHWINNNG Herbal Dietary Supplement Recalled by Today The World Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sustain Herbal Dietary Supplement Recalled by Today The World Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 with a Certeray generator -To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune's Fix Recalled by Super Chill Products Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mesalamine Extended-Release Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a...
The Issue: Their is a potential that electromagnetic interference may cause leadless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.