The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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Any3+ (High and above)4+ (High and above)5+ (High and above)

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6901–6925 of 89525

  • HighFDA (Food)·F-0837-2025·2025-06-11

    Dye-Free Frosted Sugar Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Dye-Free Frosted Sugar Cookies due to printing quality issues that failed to clearly declare allergens (egg, milk, soy) on the label. The product was distributed in Utah.

    Product
    Dye-Free Frosted Sugar Cookie: Gluten-free dye-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1895-2025·2025-06-11

    Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect

    Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.

    Product
    Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1901-2025·2025-06-11

    Access Testosterone assay Catalog Number 33560 recalled

    Beckman Coulter is recalling the Access Testosterone assay (Catalog Number 33560) due to inadequate maintenance on manufacturing equipment that caused cross-contamination in testosterone reagent packs, which could result in inaccurate patient test results.

    Product
    Access Testosterone assay, Catalog Number 33560
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1899-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.

    Product
    Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1887-2025·2025-06-11

    Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall

    Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.

    Product
    Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0007-2025·2025-06-11

    Eudos Bronquilan Recalled for Undeclared Food Color Additives

    Nature's Eudos Distributors LLC is recalling Eudos Bronquilan due to undeclared food color additives (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40). Consumers with allergies or sensitivities to these dyes should not use the product.

    Product
    Eudos Bronquilan
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0829-2025·2025-06-11

    Plain Gluten-Free Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling plain gluten-free bagels due to printing quality issues that rendered the egg allergen declaration unclear or unreadable on the label.

    Product
    Plain Bagels: Gluten-free plain bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm fruit oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum, Enzyme. Contains: Egg.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0011-2025·2025-06-11

    Giant Instant Oatmeal Raisins and Spice Recalled for Undeclared Walnuts

    Giant Instant Oatmeal Raisins and Spice is being recalled because walnuts are not declared on the outer packaging, though they appear on the inner packaging. Consumers with walnut allergies who rely on outer-package labeling are at risk.

    Product
    Giant, Instant Oatmeal Raisins and Spice, 10 -1.5 oz. Packets, per box. Net. Wt. 15.01 oz.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0830-2025·2025-06-11

    Gluten-Free Multigrain Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling gluten-free multigrain bagels due to printing defects that render the egg allergen declaration illegible on the package label. The product contains egg and poses a risk to consumers with egg allergies.

    Product
    Multigrain Bagels: Gluten-free multigrain bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Psyllium husk powder, Rice bran, Sea salt, Xanthan
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0824-2025·2025-06-11

    Gluten-Free Artisan White Bread Recall Due to Undeclared Egg Allergen

    New Grains Gluten Free Bakery is recalling approximately 41 units of Artisan White Bread due to undeclared egg allergen on the label. Poor print quality rendered the egg allergen declaration illegible or missing.

    Product
    Artisan White Bread: Gluten-free artisan white bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum. Contains: Egg.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0827-2025·2025-06-11

    Gluten-Free Blueberry Bagels Recalled for Undeclared Egg Allergen

    New Grains Gluten Free Bakery is recalling gluten-free blueberry bagels because the label does not clearly declare the egg allergen due to printing quality issues.

    Product
    Blueberry Bagels: : Gluten-free blueberry bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm fruit oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum, Enzyme. Contains: Eg
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1906-2025·2025-06-11

    Dexcom G7 iOS App version 2.7.0 stops updating glucose readings

    Dexcom G7 iOS App version 2.7.0 can enter a state where glucose readings freeze and alerts do not trigger, risking missed detection of dangerously high or low blood sugar. Other connected devices like Apple Watch and insulin pumps continue to receive glucose data directly from the transmitter.

    Product
    Dexcom G7 iOS Application, Ref: SW12300 used in conjunction with the Dexcom G7 Continuous Glucose Monitoring (CGM) system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V368000·2025-06-11

    Nova Bus turn signal indicator lights may remain solidly illuminated

    Nova Bus is recalling certain 2022-2023 LFS buses because a digital display firmware error may leave the instrument panel turn signal indicators solidly lit, failing FMVSS 108.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V331000·2025-06-10

    Hyundai Translead Recalls 2026 Dry Van Trailers for Liftgate Pin Defect

    Hyundai Translead is recalling 2026 Dry Van Trailers because insufficient lubrication on the liftgate cylinder pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DRY VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V364000·2025-06-10

    Forest River trailer side gate latches may unlock during transit

    Forest River is recalling certain 2025 Salem and Wildwood travel trailers because the side entry gate latch may unlock, allowing the strut to open the gate during transit.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V381000·2025-06-09

    Braun Recalls 1,533 Vehicles for Loose Seat Belt Fasteners

    Braun is recalling 1,533 Chrysler Pacifica, Voyager, and Toyota Sienna vehicles because seat belt tie-down fasteners may be loose, increasing injury risk in crashes.

    Product
    BRAUN — BRAUN CHRYSLER PACIFICA, CHRYSLER VOYAGER, TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V332000·2025-06-06

    Volvo Recalls 2025-2026 VN Trucks for Power Cable Routing Defect

    Volvo Trucks North America is recalling 2025-2026 Volvo VN trucks because improperly routed power cables may cause electrical shorts, leading to engine stalls or fires.

    Product
    VOLVO — VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V375000·2025-06-06

    2018–2024 Harley-Davidson Softail motorcycles rear shock issue

    Harley-Davidson is recalling certain 2018–2024 Softail motorcycles because the rear shock pre-load adjuster mounting tab may break and damage the tire, causing sudden loss of pressure and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FLHCS ANV, FXLRS, FXLRST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V379000·2025-06-06

    Mercedes-Benz GLC 300 and AMG GLC models roof impact protection

    Mercedes-Benz is recalling certain 2023–2025 GLC 300 and GLC 300 4MATIC, 2024–2025 AMG GLC 43 4MATIC, 2025 GLC 350E 4MATIC, and 2025 AMG GLC 63 S E vehicles with panoramic sunroofs. The C-pillar may not absorb adequate impact in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ REDUNDANT AMG GLC43 4MATIC, GLC 300, GLC 300 4MATIC, GLC 350 E 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25316·2025-06-05

    Portable Hook-On Chairs Recalled for Fall Hazard and Serious Injury Risk

    Portable hook-on chairs sold on Amazon by Ravmix pose a fall hazard because the crotch restraint can be removed without tools, allowing infants to fall through. The product violates federal safety standards. Consumers should stop using immediately and contact Ravmix for refund instructions.

    Product
    Portable Hook-On Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25315·2025-06-05

    ZHORANGE Portable Bassinets Recalled for Fall Hazard Risk

    ZHORANGE portable bassinets (model 148012-A) are recalled due to sides that are too low and absence of a stand, creating a fall hazard for infants. The product violates federal safety standards for infant sleep products.

    Product
    ZHORANGE Portable Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25311·2025-06-05

    BowFlex Adjustable Dumbbells Recalled Due to Dislodging Weight Plates

    About 3.8 million BowFlex 552 and 1090 adjustable dumbbells are recalled because weight plates can dislodge from the handle during use. Over 100 injuries have been reported, including concussions and broken toes.

    Product
    BowFlex 552, 52.5 LB Adjustable Dumbbells and BowFlex 1090, 90 LB Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide