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. 2,637 recalls have been distributed to Oregon in the last 12 months.
Showing 9701–9720 of 28,488 recalls
Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...
The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPTAR Laser Range Finders Recalled by Potomac River Group, Corp. Due to...
The Issue: RAPTAR units are capable of being field modified to enable the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semi-automatic Biopsy-Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrodissection Cannula (Chang) Recalled by Anodyne Surgical Due to The...
The Issue: The product may have a yellowish-brown/greenish-brown residue present at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24...
The Issue: Evaluation of a clinical goal for the voxelwise worst dose distributions may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 21 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 17 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...
The Issue: Removing parts for safety reasons due to possible breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Duodenoscope - Product Usage: intended to be Recalled...
The Issue: IFU updated: The warning section of the IFU for both the OE-A63 distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centaur Syphilis Assay-SYP Kit Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for the ADVIA Centaur Syphilis assay to carryover into other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for...
The Issue: One batch of the ELUVIATM Drug Eluting Vascular Stent System incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in...
The Issue: The lot may have experienced an anomaly during the manufacturing process,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MOSAIC Oncology Information System versions: 2.62 Recalled by Elekta,...
The Issue: Malware attack
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom RAX with software version VF10 Recalled by Siemens Medical...
The Issue: Siemens identified two issues, In some cases, it is possible to perform an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Logical cup liner - Product Usage: intended to replace a Recalled by...
The Issue: Product mislabeled, with the incorrect product inside the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.