The Recall Desk

State

Oregon product recalls

72,992 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.

These figures cover only the 7,526 recalls whose distribution notice names Oregon specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8501–8525 of 80518

  • HighNHTSA·25V006000·2025-01-13

    Kia Sorento software error may disable low beams and taillights

    Kia is recalling certain 2024-2025 Sorento vehicles because a Body Domain Control Unit software error may cause a loss of low beam headlights and taillights.

    Product
    KIA — KIA SORENTO HYBRID, SORENTO PHEV, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E001000·2025-01-13

    Nivion NSP01 Charger Adapter Recall for Electrical Arcing Risk

    N&B Mobility Solutions is recalling Nivion NSP01 charger adapters due to electrical arcing and shock risks. Owners should contact Nivion for a free replacement.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V007000·2025-01-13

    Winnebago spare tire carrier mounting bolts may loosen and detach

    Winnebago is recalling certain 2025 Minnie Winnie and Spirit motorhomes because the spare tire carrier mounting bolts may loosen, allowing the carrier to detach.

    Product
    WINNEBAGO — WINNEBAGO SPIRIT, MINNIE WINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2025·2025-01-11

    Bestway Recalls Frozen Chicken Taquitos Due to Metal Contamination

    Bestway Sandwiches Inc. is recalling frozen chicken and cheese taquitos due to possible metal contamination. One consumer reported a dental injury.

    Product
    Bestway Sandwiches Inc. — Bestway Sandwiches Inc. Recalls Frozen Chicken And Cheese Taquito Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0359-2025·2025-01-08

    Grimmway Farms Organic Baby Carrots recalled for E. coli O121 contamination

    Grimmway Farms is recalling approximately 21,094 cases of Organic Baby Carrots that may be contaminated with E. coli O121:H19. The product was distributed across 38 U.S. states, Puerto Rico, and Canada, UAE, Hong Kong, and Colombia.

    Product
    --- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Baby Carrots 25 Lbs. Grimmway Farms --- Brand --- Grimmway Farms
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Food)·F-0357-2025·2025-01-08

    Organic Baby Carrots Recalled for E. coli O121:H19 Contamination

    Grimmway Farms is recalling organic baby carrots (Cal-Organic and Marketside brands) due to potential E. coli O121:H19 contamination affecting 10,482 cases distributed across the U.S., Puerto Rico, and internationally.

    Product
    --- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz Steam-to-Serve RPC --- Brand --- Cal-Organic; Marketside
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Food)·F-0361-2025·2025-01-08

    Organic Whole Carrots Recalled for Potential E. coli O121:H19 Contamination

    Grimmway Farms is recalling approximately 4,057 cases of organic whole carrots distributed nationally due to potential E. coli O121:H19 contamination. No illnesses have been reported.

    Product
    --- Organic Whole Carrots --- Organic Clip Carrots 50 Lbs Cal-Organic Farm; Organic Clip Carrots 50 Lbs Cal-Organic RPC --- Brand --- Cal-Organic
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Food)·F-0358-2025·2025-01-08

    Organic Baby Carrots Recalled Due to E. coli Contamination Risk

    Grimmway Farms is recalling organic baby carrots sold under multiple brands due to potential E. coli O121:H19 contamination affecting approximately 218,705 cases distributed nationwide and internationally.

    Product
    --- Organic Baby Carrots --- Orangic Baby Peeled Carrots 13/3 BL; Orangic Baby Peeled Carrots 30/1 BL; Org Baby Peeled Carrots 12/2 Wholesome Pantry RPC; Org Baby Peeled Carrots 24/1 Wholesome Pantry RPC; Organic Baby Peeled Carrots 10/2/2Lb Cal O Display; Organic Baby Peeled Car
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Drugs)·D-0170-2025·2025-01-08

    FORCE FOREVER supplement tablets recalled for undisclosed drugs

    GNMart LLC is recalling FORCE FOREVER 400mg tablets nationwide after the FDA found the product contains undisclosed Diclofenac and Dexamethasone. The Class I recall affects all lots of this dietary supplement product.

    Product
    FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0373-2025·2025-01-08

    Fresh cucumbers recalled due to potential Salmonella contamination

    Baloian Farms is recalling fresh cucumbers sold under the Pamela and Stock Vegetables brands due to potential Salmonella contamination. Approximately 40,043 cases were distributed to wholesale, retail, and food service operations across 18 states.

    Product
    whole fresh American cucumbers packaged in bulk cardboard containers labeled with the "Pamela" brand, a generic white box with a sticker that provides the implicated grower's name, "Agrotato, S.A. de C.V.," or a clear PamPak branded bag of 6 individual cucumbers with the UPC 8 25
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-0360-2025·2025-01-08

    Organic Carrots Recalled Due to Potential E. coli O121:H19 Contamination

    Grimmway Enterprises is recalling organic whole and juice carrots sold under multiple brands due to potential contamination with E. coli O121:H19. The recall affects carrots distributed across the U.S., territories, and certain foreign countries.

    Product
    --- Organic Whole Carrots --- Organic Carrot 125/6 Cal-Organic Farms; Organic Carrot 150/5 Bunny Luv; Organic Carrots 10/5 Lb O-Organic; Organic Carrots 10/5 Simple Truth; Organic Carrots 10/5# 365 Organic; Organic Carrots 10/5# 365 Organic RPC; Organic Carrots 10/5# Bunny Luv;
    Category
    Food
    Distribution
    41 states
  • HighFDA (Devices)·Z-0785-2025·2025-01-08

    Medline surgical procedure kits recalled for potential endotoxin contamination

    Medline is recalling three custom surgical procedure kits due to non-sterile Codman Surgical Patties and Strips that pose a potential endotoxin contamination risk. The affected kits were distributed in the US, Canada, and the UAE.

    Product
    Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK, REF DYNJ66449.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0172-2025·2025-01-08

    Dapsone Topical Gel Recalled Due to Crystallization Defect

    Viona Pharmaceuticals is recalling Dapsone Gel 7.5% (2760 packs) distributed nationwide due to crystallization in the formulation. The voluntary recall affects lots T400514 and T400808.

    Product
    DAPSONE — DAPSONE (DAPSONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0791-2025·2025-01-08

    Medline Deep Brain Stimulation Surgical Kits Recalled for Non-Sterile Contamination

    Medline has recalled 128 Deep Brain Stimulation surgical kits for containing non-sterile Surgical Patties and Strips with potential endotoxin contamination. Affected units were distributed worldwide including the US, UAE, and Canada.

    Product
    Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2025·2025-01-08

    Medline Nasal Pack Procedure Kits Recalled for Potential Endotoxin Contamination

    Medline custom nasal pack procedure kits contain non-sterile surgical components with potential endotoxin contamination. Customers should discontinue use and contact Medline.

    Product
    Medline custom medical procedure kits labeled as: 1) NASAL PACK, REF DYNJ67789A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0321-2025·2025-01-08

    An Pan Buns Lack Sesame Allergen Declaration on Label

    Oyatsupan Bakers is recalling An Pan buns because the allergen declaration doesn't list sesame, though black sesame seeds are visible and listed in ingredients. Distribution was limited to Oregon and Washington.

    Product
    An Pan bun is a sweet roll filled with sweet red bean paste, stamped with black sesame seeds on top. Product is packaged in clear polypropylene bag, heat sealed with white labels on front and back. Net wt. 2.9pz. UPC 854077007055. The affected label states "**INGREDIENTS: Azuki
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0787-2025·2025-01-08

    Medline Surgical Procedure Kits Recalled Due to Sterility Concerns

    Medline is recalling custom surgical procedure kits that contain non-sterile surgical supplies with potential for endotoxin contamination. The kits were distributed worldwide, including the United States, United Arab Emirates, and Canada.

    Product
    Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0777-2025·2025-01-08

    Medline surgical procedure kits recalled for non-sterile supplies

    Medline is recalling custom medical procedure kits containing non-sterile surgical supplies with potential endotoxin contamination. The affected kits were distributed nationwide and internationally.

    Product
    Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF, REF DYNJ0382559M; 2) CRANI, REF DYNJ56001B; 3) GENDER AFFIRMING SURGERY, REF DYNJ66252; 4) GENDER AFFIRMING SURGERY, REF DYNJ66252A; 5) MAJOR NEURO PACK-LF, REF DYNJ0578916X.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0793-2025·2025-01-08

    Medline custom surgical procedure kits recalled for non-sterile components

    Medline is recalling 182 custom surgical procedure kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. The kits were distributed in the US, UAE, and Canada.

    Product
    Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF, REF DYNJ0867145G; 2) CERVICAL SPINE PACK HUM-LF, REF DYNJ35184F; 3) ANTERIOR CERVICAL-CORPECTOMY, REF DYNJ904827.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0778-2025·2025-01-08

    Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk

    Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.

    Product
    Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0792-2025·2025-01-08

    Medline Medical Procedure Kits Recalled for Non-Sterile Component Contamination

    Medline Industries is recalling 2,664 custom medical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The affected kits were distributed in the US, UAE, and Canada.

    Product
    Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V004000·2025-01-08

    Blue Bird Recalls 2025 All American Bus for Wiring Defect

    Blue Bird is recalling one 2025 All American transit bus because incorrect wiring reverses high and low beams, potentially blinding other drivers.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide