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. 1,810 recalls have been distributed to Oregon in the last 12 months.
Showing 34601–34620 of 50,914 recalls
Recalled Item: Peas & Carrots Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...
The Issue: Peas & Carrots are recalled because they have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mini Bow Tie Pasta and Vegetable Blend Recalled by CRF Frozen Foods, LLC Due...
The Issue: Mini Bow Tie Pasta and Vegetable Blend is recalled because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Root Medley Recalled by CRF Frozen Foods, LLC Due to Potential...
The Issue: Organic Root Medley is recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Werner Brand Butter Toffee Peanuts Recalled by Werner Gourmet Meat Snacks,...
The Issue: Werner Brand Butter Toffee Peanuts are recalled because the labels declared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Werner Brand Sweet Hot Crunch Mix Recalled by Werner Gourmet Meat Snacks,...
The Issue: Werner Brand Sweet Hot Crunch Mix is recalled because label declared butter,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One...
The Issue: One of the dent markers from the DX-D600 dropped down from the overhead rail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diet Dr Pepper Recalled by Coca-Cola Company (The) Due to In a small...
The Issue: In a small percentage of the cans, when opened, the oval covering for the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coca-Cola Recalled by Coca-Cola Company (The) Due to In a small percentage...
The Issue: In a small percentage of the cans, when opened, the oval covering for the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sprite Zero Recalled by Coca-Cola Company (The) Due to In a small percentage...
The Issue: In a small percentage of the cans, when opened, the oval covering for the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...
The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.