State
73,486 recalls have nationwide distribution and so reach Oregon. 7,533 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,533 recalls naming Oregon we have scored against our rubric, 876 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,128 (28%) are Severe.
Which agencies issued them
These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
bioMerieux is recalling VIDAS Measles IgG test kits due to a substrate error that prevents the test from running, requiring users to repeat testing and potentially delaying results.
Native Creation is recalling approximately 170 small wool sweaters for children sizes 0 to 8 because the zipper pull contains lead paint that exceeds federal limits and poses a toxic ingestion risk to young children.
Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution USP 4% due to superpotency. The affected lot was distributed nationwide.
bioMerieux VIDAS LH test kits (lot 1008848600) are affected by a substrate error that prevents test execution, requiring users to repeat testing and potentially delaying results.
A diagnostic test kit manufactured by bioMerieux has been recalled because a substrate error prevents the test from running, which delays test results for patients.
bioMerieux is recalling 1,579 VIDAS DEX@ diagnostic devices due to substrate errors that prevent test execution, requiring users to rerun tests and potentially delaying results.
Biomerieux is recalling RAPID 20 E diagnostic systems because the package insert contains an incorrect color for interpreting negative CIT test results.
bioMerieux is recalling one lot of VIDAS SARS-CoV-2 IgM tests nationwide due to a substrate defect that prevents the test from running. The defect causes delayed results as users must repeat testing.
Teligent Pharma is recalling Betamethasone Dipropionate Lotion USP 0.05% (Augmented) due to failure to meet specification for the Active Pharmaceutical Ingredient particle test during routine stability testing.
bioMerieux is recalling VIDAS FSH test kits due to substrate errors that prevent the test from running, requiring repeated testing and delaying results.
bioMerieux is recalling three lots of VIDAS Lyme IgM II diagnostic test kits due to a substrate error that prevents the test from running, requiring users to conduct another test to obtain results.
bioMerieux is recalling three lots of VIDAS RUB IgG test kits due to substrate errors that prevent the test from running, potentially delaying diagnostic results.
bioMerieux is recalling 1,818 units of VIDAS PRG Progesterone test kits due to a substrate error that prevents the tests from running properly, causing delayed results when patients need repeat testing.
LGS Industries is recalling 2014-2021 trailers because the electric rear door winch cable may break, allowing the door to fall open and increasing injury risk.
Rosenbauer America is recalling 2018-2022 fire trucks because fuel tubes may crack, causing high-pressure leaks that could lead to fire.
Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.
Efficient Laboratories is recalling approximately 4,026 bottles of Rompe Pecho Max Multi-Symptoms cough and cold medicine nationwide due to potential microbial contamination of the non-sterile product.
Efficient Laboratories is recalling Rompe Pecho guaifenesin expectorant in 4 fl oz and 6 fl oz bottles due to microbial contamination of non-sterile products. The affected product was distributed nationwide.
Stealthstation and Synergy Cranial surgical navigation systems may display an incorrect biopsy needle position due to software synchronization failure. This could result in prolonged surgery, additional procedures, or tissue injury.
GIVE AND GO is recalling NL two-bite Cream Cheese Iced Cinnamon Rolls nationwide due to potential metal contamination in the product.
Maquet Cardiovascular is recalling Hemashield Gold vascular grafts due to probable mislabeling. A different graft product may have been packaged in the carton.
GIVE AND GO is recalling two-bite apple caramel cupcakes (10 oz., UPC 770981055503) nationwide due to potential metal contamination in the product.
Wright Medical recalled 22 units of CHARLOTTE MTP Hex Screws with incorrect product in packaging. Affected lots 02010697711582590 and 02010697711582591 were distributed to surgical facilities in the US, Canada, Australia, Spain, UK, and Chile.
Give and Go is recalling two-bite vanilla cupcakes nationwide due to potential metal contamination in the product. Consumers should stop using affected units and contact the manufacturer.
GIVE AND GO is recalling Favorite Day Bakery Frosted Sugar Cookies (13.5 oz., UPC 0 85239 41050 9) distributed nationwide due to potential metal contamination in the product.