State
72,919 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,525 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 1,803 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,525 recalls whose distribution notice names Oregon specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Merit Medical is recalling the 16F Dual Valved Splittable Sheath Introducer in bulk non-sterile form because a design defect may prevent it splitting as intended.
Philips Respironics is recalling the Trilogy Evo ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Merit Medical is recalling CentrosFLO Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-411 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-401 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Merit Medical is recalling ProGuide Chronic Dialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Merit Medical is recalling BioFlo DuraMax Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.
I.T.S. GmbH is recalling the Humeral Head Plate with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Ajinomoto Foods North America Inc. is recalling Ajinomoto Vegetable Gyoza Dumplings due to the presence of glass fragments in the product. The recalled dumplings were distributed nationwide.
Olympus is recalling Everest Bipolar Cutting Forceps model 3005 because a supplier did not adequately validate the welding process, and defective welds can cause the jaw to break during clinical use.
Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.
Mangalm LLC is recalling Tops GOLD Khatta Meetha Pickle due to potential adulteration with erucic acid from the mustard oil ingredient. The 33.51 oz cans were distributed in California, Nevada, Oregon, Utah, and Washington.
Ajinomoto Foods North America Inc. is recalling Item 5650893 Japanese-Style Vegetable Fried Rice because some packages may contain glass fragments measuring 1–3 cm long and 2–4 mm wide.
Ajinomoto Foods North America Inc. is recalling Ajinomoto Golden Tiger Vegetable Fried Rice due to the presence of glass fragments varying from 1–3 cm long and 2–4 mm wide in the product.
Olympus is recalling HALO PKS Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Teva is recalling nine lots of Octreotide Acetate for Injectable Suspension 20 mg after quality system deficiencies were identified during an FDA inspection at the contract manufacturer.
Beckman Coulter is recalling one lot of MicroScan Neg MIC 56 panels due to the likely presence of contamination in one or more wells.
Olympus is recalling the OER-Elite Endoscope Reprocessor because the MAJ-1443 and MAJ-1444 air/water valves are no longer reprocessing compatible with the OER-Pro and OER-Elite reprocessors.
I.T.S. GmbH is recalling Straight Plates with Angular Stability, including forearm and compression plates, because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
I.T.S. GmbH is recalling the I.T.S. Screw System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
I.T.S. GmbH is recalling the Pelvic Reconstruction System PRS RX and PRS Phoenix because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Olympus is recalling PKS Cutting Forceps model 3005PK because a supplier did not adequately validate the welding process and defective welds can cause the jaw to break during clinical use.
I.T.S. GmbH is recalling the LRS Locking Reconstruction System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.