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.
Showing 36161–36180 of 50,914 recalls
Recalled Item: Syngo Plaza Picture archiving and communication system. Software only. PACS...
The Issue: Siemens is releasing an updated software version to address several software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STD KIT GK260 Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CA500 Epix Universal Clip Applier Product Usage: The Epix disposable...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...
The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...
The Issue: Metal shavings released from burs during use are due to contact between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.