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. 2,420 recalls have been distributed to Oregon in the last 12 months.
Showing 41561–41580 of 50,914 recalls
Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Printouts...
The Issue: Printouts may be printed in incorrect anatomical size when using syngo.plaza...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps Sterile RX Recalled by...
The Issue: The product is sold and labeled as EO sterilized, however the units were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Recalled by Cure Medical LLC Due to Some of the intermediate boxes...
The Issue: Some of the intermediate boxes within lot 140417-3, were labeled as P8, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...
The Issue: Defective container: A customer complaint revealed the presence of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Salpica 11.5 oz. Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 16 oz. Jalapeno Jack Queso Dip Recalled by Riba Foods Inc Due to...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Black Bean Nacho Recalled by Riba Foods Inc Due to Undeclared...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crate & Barrel 11.5 oz. Monterey Jack Queso Dip Recalled by Riba Foods Inc...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arriba! 16 oz. Chili Con Queso-Hot Recalled by Riba Foods Inc Due to...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Ballpark Nacho Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...
The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Cabinet X-ray systems Recalled by GE Inspection Technologies, LP Due to...
The Issue: GE discovered these cabinet x-ray systems' potential failure to comply with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.