The Recall Desk

State

Oregon product recalls

72,971 recalls have nationwide distribution and so reach Oregon. 7,526 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,526
Critical
876
Severe
1,803
Most recent
2026-09-16

Of the 7,526 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 7,526 recalls whose distribution notice names Oregon specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6526–6550 of 80497

  • HighFDA (Devices)·Z-1927-2025·2025-06-18

    EPIONE Stereotactic Device Software Bug Poses Instrument Guidance Risk

    The EPIONE Model 30-0001 stereotactic device is recalled due to a software bug that may cause the robotic arm to incorrectly guide surgical instruments during CT-guided ablation procedures. Four units have been distributed in the U.S.

    Product
    EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0460-2025·2025-06-18

    Celecoxib Capsules Recalled for Foreign Tablet Contamination

    AvKARE is recalling Celecoxib 200 mg capsules because one tadalafil 5 mg tablet was found in a 500-count bottle. The contamination poses a risk of unintended drug exposure to patients.

    Product
    CELECOXIB — CELECOXIB (CELECOXIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1925-2025·2025-06-18

    Digital Acquisition Box Electrode Placement Labels Applied Backwards

    Natus Neurology has recalled the OBM00002 OBM DAB (Digital Acquisition Box) because electrode placement labels were applied backwards. This may lead to misdiagnosis of seizure location in neonates monitored with the device.

    Product
    Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25C008000·2025-06-18

    Evenflo Recalls Titan 65 Child Seats Due to Incorrect Instruction Manuals

    Evenflo is recalling Titan 65 child seats manufactured in early 2025 that may have incorrect instruction manuals, posing a risk of improper installation.

    Product
    EQUIPMENT:OTHER:OWNERS/SERVICE/OTHER MANUAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1926-2025·2025-06-18

    DxI 9000 Access Immunoassay Analyzer software version 1.20 recall

    Beckman Coulter is recalling certain DxI 9000 Access Immunoassay Analyzers due to incorrect motor/encoder and cable installation that causes error codes, prevents assays from running, and delays result generation.

    Product
    DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software versions 1.20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1968-2025·2025-06-18

    Guardian System 2 Controller units recalled for battery alert display defect

    Turncare has recalled certain Guardian 2 System controllers because a software issue prevented "low" and "terminal" battery alerts from displaying on the screen in specific circumstances when the device was not running patient therapy.

    Product
    Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software Version: 2.5.4-69 (Fix)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0461-2025·2025-06-18

    Chlorthalidone Tablets Recalled Due to Failed Dissolution Specifications

    AvKARE is recalling Chlorthalidone Tablets USP 25 mg due to failed dissolution specifications. The defect may affect the drug's therapeutic effectiveness.

    Product
    CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0933-2025·2025-06-18

    Instant Milk Tea Matcha Flavor recalled for undeclared milk allergen

    R&M Refresher Instant Milk Tea Matcha Flavor is recalled because its label declares "Non-Dairy Creamer" but does not specify that the product contains milk (whey powder and sodium caseinate). The product may cause allergic reactions in consumers with milk allergies.

    Product
    Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71Y85TG 3-pack ASIN #B0D71YBV1X Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1947-2025·2025-06-18

    Thermo SCIENTIFIC Sensititre Mueller-Hinton Broth diagnostic device recalled

    Remel, Inc. is recalling one lot of Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth due to off-color that may affect performance of this in-vitro diagnostic device.

    Product
    Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0469-2025·2025-06-18

    Cephalexin Oral Suspension Recalled for Failed Impurities Specifications

    Ascend Laboratories is recalling Cephalexin for Oral Suspension due to an out-of-specification result in impurity testing that identified Cephalexin Glucose Adduct during stability analysis.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0932-2025·2025-06-18

    Instant Milk Tea Taro Flavor Recalled for Undeclared Milk Allergen

    R&M Refresher brand Instant Milk Tea Powder in Taro Flavor is recalled nationwide because the label does not declare milk, though the product contains Whey Powder and Sodium Caseinate derived from milk.

    Product
    Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D72CMLBH 3-pack ASIN #B0D72D6589 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1967-2025·2025-06-18

    Guardian System 2 Controller Software Battery Alert Display Issue

    Turncare is recalling Guardian System 2 Controllers due to a software issue where low and terminal battery alerts do not display on the screen in certain circumstances when the device is not running patient therapy.

    Product
    Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software Version: 2.5.4-59 (Fix)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0468-2025·2025-06-18

    Cephalexin Oral Suspension Recalled for Failed Impurity Specifications

    Ascend Laboratories is recalling Cephalexin for Oral Suspension due to failed impurity specifications identified during stability testing. An out-of-specification result for Cephalexin Glucose Adduct was observed at six months.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1964-2025·2025-06-18

    Baxter Novum IQ Syringe Pump Design Issue Recall

    Baxter is recalling certain Novum IQ Syringe Pumps manufactured or repaired after July 4, 2023, due to a design issue that may falsely detect a syringe flange when none is loaded, causing the pump interface to become stuck or display a System Error 21502.

    Product
    Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1937-2025·2025-06-18

    BD BBL CultureSwab EZ Collection and Transport System Swabs Breakage

    BD BBL CultureSwab EZ Collection and Transport System (REF 220144) is being recalled because swabs may break during use. The recall affects units distributed nationwide in Maryland.

    Product
    BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0470-2025·2025-06-18

    Levothyroxine Sodium tablets recalled for foreign substance contamination

    Macleods Pharmaceuticals is recalling Levothyroxine Sodium 112 mcg tablets (Lot #MLF2401A, expiration 01/31/2026) distributed nationwide due to black hair found embedded in tablets.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0462-2025·2025-06-18

    Ezetimibe and Simvastatin Tablets Recalled for Failed Impurity Specifications

    Glenmark Pharmaceuticals Inc., USA is recalling Ezetimibe and Simvastatin Tablets (10mg/40mg) due to out-of-specification results for related substances in a stability study. The recall affects approximately 6,759 bottles distributed nationwide.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0936-2025·2025-06-18

    NOW Nutritional Yeast Powder recalled due to packaging error

    NOW Foods is recalling NOW Nutritional Yeast Powder (10 oz, UPC 7 33739 02460 2) because regular yeast was inadvertently packaged as nutritional yeast.

    Product
    NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 02460 2
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V401000·2025-06-13

    Ford Super Duty brake pushrod springs missing; owners told not to drive

    Ford is recalling certain 2025 Super Duty trucks because the brake booster pushrod retaining spring may not have been installed, risking sudden loss of brake function.

    Product
    FORD — FORD F-250 SD, F-350 SD, F-450 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V394000·2025-06-13

    Ford Recalls 2025 Mustang Mach E for Transmission Park Rod Defect

    Ford is recalling 2025 Mustang Mach E vehicles because the transmission park rod may fail to engage, creating a risk of vehicle rollaway and crash.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V403000·2025-06-13

    Lincoln Navigator side marker and daytime running lights may fail

    Ford is recalling certain 2022 Lincoln Navigator vehicles previously repaired under recall 22V455 because headlight control module software may fail the side marker and daytime running lights.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide