The Recall Desk

State

Oregon product recalls

72,919 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,525
Critical
876
Severe
1,803
Most recent
2026-09-09

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.

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.

2601–2625 of 80444

  • HighFDA (Devices)·Z-1685-2026·2026-04-08

    Artoura textured tissue expander infusion set needles may be blunt

    Mentor is recalling textured Artoura Breast Tissue Expanders with integral injection dome because the infusion sets may contain a dull or blunt needle tip.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2026·2026-04-08

    Philips Allura Xper FD20/15 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20/15 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/15 OR Table; System Code: 722059;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2026·2026-04-08

    CPX 4 low height tissue expander infusion needles may be blunt

    Mentor is recalling the CPX 4 US Breast Tissue Expander with Suture Tabs, smooth low height 650 cc, because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH Smooth Low Height Tissue Expander, 650cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1665-2026·2026-04-08

    Philips Allura Xper FD20 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2026·2026-04-08

    CPX 4 medium height tissue expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth medium height range because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1745-2026·2026-04-08

    MiniMed 720G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 720G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1741-2026·2026-04-08

    MiniMed 780G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 780G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1674-2026·2026-04-08

    Philips Azurion 3 M15 X-ray may not start from foot switch

    Philips is recalling the Azurion 3 M15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1761-2026·2026-04-08

    Burlington Medical leg wraps may lose radiation attenuation over time

    Burlington Medical is recalling leg wraps because of the potential for attenuation degradation over time, decreasing the lifespan of the product.

    Product
    Burlington Medical, Leg Wraps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2026·2026-04-08

    CPX 4 tall height tissue expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth tall height range because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH, SCPX-123TH, SCPX-140TH, SCPX-146TH Smooth Tall Height Tissue Expander, 350cc, 450cc, 650cc, 750cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0420-2026·2026-04-08

    Prazosin hydrochloride tablets recalled over nitrosamine impurity above limits

    Five lots of Prazosin Hydrochloride tablets are being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.

    Product
    PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1681-2026·2026-04-08

    CPX 4 SILTEX low height expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the SILTEX low height range because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1698-2026·2026-04-08

    da Vinci mega needle driver recalled over broken or frayed cables

    Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0641-2026·2026-04-08

    Roasted peanuts recalled for undeclared banned sweetener cyclamate

    Mei Heong Yuen tangerine flavor roasted peanuts are recalled because they contain cyclamate, a sweetener banned in the U.S.

    Product
    MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super Wor
    Category
    Food
    Distribution
    19 states
  • ModerateNHTSA·26V221000·2026-04-08

    Forest River Recalls 2026 Travel Trailers Due to Incorrect Weight Labeling

    Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER AVENGER, WESTBROOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0643-2026·2026-04-08

    Mei Heong Yuen Garlic Flavor Roasted Peanuts Recalled for Banned Sweetener

    Mei Heong Yuen Garlic Flavor Roasted Peanuts (9.17 oz) are being recalled because they contain cyclamates, a banned sweetener. The product was distributed across multiple states.

    Product
    MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; U
    Category
    Food
    Distribution
    19 states
  • LowFDA (Food)·H-0642-2026·2026-04-08

    Mei Heong Yuen Walnut Flavor Roasted Peanuts recalled for banned sweetener

    Super World Trading Inc. is recalling Mei Heong Yuen Walnut Flavor Roasted Peanuts (9.17 oz) because the product contains cyclamates, a sweetener banned in the United States.

    Product
    MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Liquorice, Sugar, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trad
    Category
    Food
    Distribution
    19 states
  • HighNHTSA·26V218000·2026-04-06

    2024 Genesis G90 seat belt anchors may detach in crash

    Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI, GENESIS SANTA FE HYBRID, IONIQ 6, SANTA FE, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V217000·2026-04-06

    Pierce Recalls Firetrucks Due to Faulty Stabilizer Indicator Light

    Pierce Manufacturing is recalling 2015-2026 aerial firetrucks because a faulty light may falsely indicate the vehicle is stable, increasing injury risk during operation.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, ARROW XT, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V219000·2026-04-06

    Greenpower Recalls School Buses Due to Missing Mirror Warning Label

    Greenpower is recalling 2020-2024 Nano Beast and 2021-2024 Beast school buses because a warning label on the cross-view mirror may be missing, potentially increasing crash risk.

    Product
    GREENPOWER — GREENPOWER NANO BEAST SCHOOL BUS, BEAST SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·PHA-04012026-01·2026-04-06

    USDA Retracts Lead Alert for Dorada Chicken Nuggets

    USDA FSIS retracted a public health alert for Dorada chicken nuggets after follow-up testing confirmed the initial lead result was a laboratory error.

    Product
    Dorada Foods — FSIS Retracts Public Health Alert for Frozen, Ready-to-Eat Chicken Nuggets Due to Updated Laboratory Result
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V216000·2026-04-03

    Mercedes-Benz Recalls Vehicles for Drive Shaft Universal Joint Breakage Risk

    Mercedes-Benz is recalling specific 2018-2020 E-Class and S-Class models because the drive shaft universal joint may break, causing a sudden loss of drive power and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 560 4MATIC COUPE, E 450 4MATIC, E 400 4MATIC, E 400 4MATIC CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide