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. 1,007 recalls have been distributed to Oregon in the last 12 months.
Showing 33601–33620 of 50,914 recalls
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molly's Kitchen Hotzzarella Cheese Sticks Recalled by Ajinomoto Windsor...
The Issue: Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poppers brand Mozzarella Cheese Sticks Net Wt. 32 oz. (2 Recalled by...
The Issue: Monogram Appetizers is recalling Poppers Brand Mozzarella Cheese Sticks...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in...
The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fire roasted Poblano & Jalapeno popper bites packaged in a Recalled by...
The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta...
The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...
The Issue: Software malfunction; The action being taken due to the device becoming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trokendi XR (topiramate) extended-release capsule Recalled by Supernus...
The Issue: Superpotent Drug: Failure of assay specifications in the capsule.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis Inc...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA PROTEIN VANILLA¿ 948 grams Recalled by HVL, LLC Due to Product...
The Issue: Product labeling does not declare milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: METABOLIC CLEASNSE VEG 1151 grams Recalled by HVL, LLC Due to Product...
The Issue: Product labeling does not declare milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: METABOLIC CLEANSE REVISED 1181 grams Recalled by HVL, LLC Due to Product...
The Issue: Product labeling does not declare milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Option-vf Urinary Catheter. Female use only. Latex Free. Sterile Recalled by...
The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.