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. 2,432 recalls have been distributed to Oregon in the last 12 months.
Showing 37921–37940 of 50,914 recalls
Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that...
The Issue: The devices that included the OVAR research test were not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phentermine Hydrochloride Capsules Recalled by PD-Rx 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: Verapamil Hydrochloride Extended-Release tablets Recalled by Apotex Inc. Due...
The Issue: Failed Dissolution Specification: One lot of product did not meet the first...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALLOPURINOL TABLETS Recalled by Qualitest Pharmaceuticals Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Titan Spine Endoskeleton Locking Bone Screw Assembly Recalled by TITAN...
The Issue: Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0/4.0 Cannulated Drill Bit Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concave Reamer Head Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the Concave and Convex Reamer Heads may be too small to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE Recalled by...
The Issue: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Waste Management System Docking Station (120V and 230V) Recalled...
The Issue: The Fluid Coupling Sleeve, a component within the Neptune Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and...
The Issue: The cutting efficiency of the Countersinks was out of specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wall Chart for STERRAD 100NX System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery LS Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery ST 16 Recalled by GE Healthcare Due to Potential for expulsion...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightspeed 16 CT Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip...
The Issue: Kale Crisps Zen Nori is recalled due to undeclared SOY. Soybean is a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vegetable Crisps Lemon Parmesan sold under brand Veggie Evolution Recalled...
The Issue: Vegetable Crisps Lemon Parmesan is recalled because label declared Parmesan...
Recommended Action: Do not consume. Return to store for a refund or discard.