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. 2,641 recalls have been distributed to Oregon in the last 12 months.
Showing 8661–8680 of 50,914 recalls
Recalled Item: Endometrin (progesterone) Vaginal Insert 100mg Recalled by Ferring...
The Issue: cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lysteda (tranexamic acid) USP Tablets Recalled by Amring Pharmaceuticals Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Havasu Beetroot Powder Recalled by Supplement Manufacturing Partner, Inc....
The Issue: Contains undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. X-ray Image guided Therapy System. Recalled by PHILIPS...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 and FD20. X-ray Imaging System. Recalled by PHILIPS MEDICAL...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxylog 3000 Plus emergency and transport ventilator Recalled by Draeger...
The Issue: Draeger has become aware of instances where the device stopped working when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Amplatzer Steerable Delivery Sheath (ASDS) Recalled by Abbott Due to...
The Issue: There is an overall reported incidence rate of 0.77% related to observed or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi/X Tip-Up Fenestrated Grasper Recalled by Intuitive Surgical,...
The Issue: Fenestrated Graspers have a manufacturing issue has the potential to cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Short Recalled by Tornier, Inc Due...
The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Recalled by Tornier, Inc Due to A...
The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sun Wave Brand Jelly Cup (Lychee Flavor) Recalled by Richin Trading Inc Due...
The Issue: Potential choking hazard
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sun Wave Brand Jelly Cup (Mango Flavor) Recalled by Richin Trading Inc Due...
The Issue: Potential choking hazard
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sun Wave Brand Jelly Cup (Assorted Flavors) Recalled by Richin Trading Inc...
The Issue: Potential choking hazard
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Churritos Corn Flour sticks Recalled by Botanas Michoacanas Due to The...
The Issue: The product labels include a Contains statement that did not disclose sesame...
Recommended Action: Do not consume. Return to store for a refund or discard.