The Recall Desk

State

Oregon product recalls

72,907 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.

Which agencies issued them

These figures cover only the 7,525 recalls whose distribution notice names Oregon specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1501–1525 of 80432

  • HighFDA (Devices)·Z-2292-2026·2026-06-10

    Arvis Hip and Knee 3.0 trackers may show wear and corrosion

    Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.

    Product
    Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0968-2026·2026-06-10

    Albertsons gourmet Dubai cookies do not declare pistachio

    Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.

    Product
    UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0566-2026·2026-06-10

    CareOne ultra strength antacid tablets contain small metallic particles

    CareOne Ultra Strength Calcium Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    ULTRA STRENGTH ANTACID ASSORTED BERRIES — ULTRA STRENGTH ANTACID ASSORTED BERRIES (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0900-2026·2026-06-10

    Bulk betaine anhydrous may contain carbon steel foreign material

    Betaine Anhydrous 98% distributed by Creative Compounds is being recalled because of possible carbon steel foreign material of 1 to 2 mm. 2,055 kg are affected.

    Product
    Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE ANHYDROUS 98%***Distributed by Creative Compounds, LLC Scott City, Missouri USA 63780***"
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2307-2026·2026-06-10

    Aligned Medical fluids kits contain recalled lidocaine injection

    Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.

    Product
    Aligned Medical AMS16835 Fluids Kit RX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1013-2026·2026-06-10

    Albertsons seafood salad contains statement does not declare crab

    Albertsons store-made seafood salad is being recalled because the contains statement does not declare crab. 114 units are affected.

    Product
    UPC 23625000000 FISH HOUSE PREMIUM SEAFOOD SALAD UPC 21431200000 Ready Meals SALAD SEAFOOD SS UPC 21878600000 SALAD SEAFOOD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0992-2026·2026-06-10

    Albertsons elegant charcuterie tray does not declare pistachio allergen

    Albertsons store-made Tray Charcuterie Elegant is being recalled because the contains statement does not declare pistachio. Eight units are affected.

    Product
    UPC 29138800000 TRAY CHARCUTERIE ELEGANT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2291-2026·2026-06-10

    Philips Azurion 7M20 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0958-2026·2026-06-10

    Albertsons colossal Dubai cheesecake slice does not declare pistachio

    Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.

    Product
    UPC 25216200000 Cheesecake Slice Colossal Dubai. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2284-2026·2026-06-10

    Philips Azurion 3M12 Roadmap Pro may produce unusable dark images

    Philips Azurion 3M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1022-2026·2026-06-10

    Albertsons fresh berry and chicken salad does not declare walnut

    Albertsons store-made Ready Meals Salad Fresh Berry & Chicken is being recalled because the contains statement does not declare walnut. 228 units are affected.

    Product
    UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0954-2026·2026-06-10

    Albertsons carrot cakes do not declare pecan or walnut

    Albertsons store-made 8-inch two-layer carrot cakes are being recalled because the contains statement does not declare pecan or walnut. 167 units are affected.

    Product
    UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE CARROT 8IN 2-Layer These are Albertson's store-made items and sold by unit at point of sale with grocery store's scale labels.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0574-2026·2026-06-10

    GoodSense antacid chewable tablets contain small metallic particles

    GoodSense Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of a foreign substance: small metallic particles in the chewable tablets.

    Product
    GOODSENSE EXTRA STRENGTH ANTACID — GOODSENSE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0960-2026·2026-06-10

    Albertsons white strawberry cake bars do not declare almond

    Albertsons store-made Artisan White Strawberry Cake Bar is being recalled because the contains statement does not declare almond. 173 units are affected.

    Product
    UPC 22253500000 Cake Bar Artisan White Strawberry Small. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2299-2026·2026-06-10

    BD Pyxis Anesthesia Station fingerprint scanner may overheat and burn

    The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.

    Product
    BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0562-2026·2026-06-10

    Casey's extra strength antacid tablets contain small metallic particles

    Casey's Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles in the tablets.

    Product
    Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2302-2026·2026-06-10

    BD Pyxis MedStation fingerprint scanners may overheat and cause burns

    BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0573-2026·2026-06-10

    H-E-B extra strength antacid tablets contain small metallic particles

    H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HEB EXTRA STREGTH ANTACID — HEB EXTRA STREGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0560-2026·2026-06-10

    Good Neighbor Pharmacy antacid tablets contain small metallic particles

    Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles.

    Product
    GOOD NEIGHBOR PHARMACY ANTACID — GOOD NEIGHBOR PHARMACY ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0569-2026·2026-06-10

    Family Wellness ultra strength antacid tablets contain metallic particles

    A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.

    Product
    FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2295-2026·2026-06-10

    Phothera 200 phototherapy calibration certificates had outputs reversed

    Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.

    Product
    Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0570-2026·2026-06-10

    Harris Teeter ultra strength antacid tablets contain metallic particles

    Harris Teeter Ultra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    Harris Teeter, ULTRA STRENGTH ANTACID, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, Distributed by: Harris Teeter, LLC.,MATTHEWS, NC 28105, UPC: 0 72036-73108-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2288-2026·2026-06-10

    Philips Azurion 7B12 Roadmap Pro may produce unusable dark images

    Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2287-2026·2026-06-10

    Philips Azurion 5M20 Roadmap Pro may produce unusable dark images

    Philips Azurion 5M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide