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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1001–1025 of 36490

  • SevereNHTSA·26V160000·2026-03-17

    2026 Hyundai Palisade power rear seats may fail to detect occupants

    Hyundai is recalling 2026 Palisade and Palisade Hybrid vehicles with Limited or Calligraphy trim because the second and third row power seats may fail to detect a person and continue moving, risking entrapment or injury.

    Product
    HYUNDAI — HYUNDAI PALISADE HYBRID, PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V151000·2026-03-13

    New Flyer Recalls Transit Buses Due to Inverter Software Error

    New Flyer is recalling certain 2021-2026 transit buses because an inverter software error may cause unintended acceleration or deceleration.

    Product
    NEW FLYER — NEW FLYER XHE40, XHE60, XE35, XE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V146000·2026-03-12

    Honda motorcycle handlebar lock screw may loosen and detach

    Honda is recalling certain 2023-2025 CMX300, CMX500 and CL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.

    Product
    HONDA — HONDA CMX300, SCL500, CMX500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V141000·2026-03-12

    Jeep Wagoneer S liftgate hinge cover may detach from vehicle

    Chrysler is recalling certain 2024-2026 Jeep Wagoneer S vehicles because the liftgate hinge cover may not be properly clipped into position and may detach from the vehicle.

    Product
    JEEP — JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V143000·2026-03-12

    Rolls-Royce Cullinan Recalled for Loose Rear Seat Bolts

    BMW of North America is recalling 2020-2026 Rolls-Royce Cullinan vehicles because loose rear seat bolts may damage seat belts or allow backrests to move.

    Product
    ROLLS-ROYCE — ROLLS-ROYCE CULLINAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1469-2026·2026-03-11

    Abiomed Impella RP with SmartAssist recalled as Class I

    Abiomed is recalling the Impella RP with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP with SmartAssist. Product Code: 0046-0035.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1471-2026·2026-03-11

    Abiomed Impella RP recalled as Class I over sensor malfunction risk

    Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP. Product Code: 0046-0011.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0397-2026·2026-03-11

    MR. 7 Super capsules recalled as Class I over undeclared sildenafil

    StuffbyNainax is recalling MR. 7 SUPER 700000 capsules because FDA analysis revealed the presence of undeclared sildenafil and tadalafil. The FDA has classified this recall as Class I.

    Product
    MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0396-2026·2026-03-11

    Mojo Max Fusion capsules recalled as Class I over undeclared drug ingredients

    Mojo Max Fusion XXX capsules are being recalled because FDA analysis revealed undeclared sildenafil at 13.1 mg per capsule and tadalafil at 13.8 mg per capsule. The FDA has classified this recall as Class I.

    Product
    Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0620-2026·2026-03-11

    Lobster and Crab Ravioli recalled for undeclared allergens

    Perfect Pasta, Incorporated is recalling Lobster & Crab Ravioli due to undeclared shrimp, crab, lobster, pollock, whiting, and soy. The product was distributed to consignees in Utah only.

    Product
    Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs, Milk, Crustaceans-Shellfish. Product is intended to be further cooked. Weight: 1-10 pound (4.5g). Use within 6 months. 801-541-9292-www.FunarosPerfectPasta.com. 1391 So. 300 West Slc, Ut 84115.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1470-2026·2026-03-11

    Abiomed Impella RP Flex recalled as Class I over sensor drift

    Abiomed is recalling the Impella RP Flex with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP Flex with SmartAssist. Product Code: 1000323.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0388-2026·2026-03-11

    Silintan herbal pills recalled as Class I for undeclared meloxicam

    123Herbals is recalling Silintan 25-count pill bottles because FDA analysis revealed the presence of undeclared meloxicam. The FDA has classified this recall as Class I.

    Product
    SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V140000·2026-03-11

    ATC travel trailer generator exhaust vents under the slide-out bedroom

    Aluminum Trailer Company is recalling certain 2023-2026 PL700 and PL750 recreational trailers because the generator exhaust is vented directly under the slide-out bedroom, letting carbon monoxide enter the cabin.

    Product
    ATC — ATC PL750, PL700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V131000·2026-03-05

    Forest River Recalls 2026 Dynamax Motorhomes Due to Electrical Bonding Defect

    Forest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes because the distribution panel may not be properly bonded to the chassis ground, posing a risk of injury or electrocution.

    Product
    DYNAMAX — DYNAMAX GRAND SPORT GT, EUROPA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V128000·2026-03-05

    Toyota Highlander second-row seat backs may fail to lock

    Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.

    Product
    TOYOTA — TOYOTA HIGHLANDER, HIGHLANDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V129000·2026-03-05

    GM heavy duty pickup fuel pump may cause an engine stall

    GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0522-2026·2026-03-04

    Frozen Blueberries Recalled Due to Listeria Contamination

    Oregon Potato Company LLC is recalling IQF blueberries due to Listeria monocytogenes contamination. The product was distributed in MI, OR, WA, WI and in Canada.

    Product
    IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged in polyethylene liner within a Gaylord 1400lbs. tote. Product was not sold to consumers from retail stores. Willamette Valley Fru
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0530-2026·2026-03-04

    Frozen fish balls 200g recalled as Class I for undeclared allergens

    Min Jiang Food Store, trading as Koi Koi Trading, is recalling frozen Fish Ball in 200 g packs because of undeclared wheat and sesame. The FDA has classified this recall as Class I.

    Product
    Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0531-2026·2026-03-04

    Frozen fish balls recalled as Class I for undeclared wheat and sesame

    Min Jiang Food Store, trading as Koi Koi Trading, is recalling frozen Fish Ball in 400 g packs because of undeclared wheat and sesame. The FDA has classified this recall as Class I.

    Product
    Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0519-2026·2026-03-04

    Dried croaker fish recalled as Class I because it is uneviscerated

    Prime Food Processing is recalling Dried Croaker Fish, 8 oz, because the fish is uneviscerated. The FDA has classified this recall as Class I, its most serious category.

    Product
    Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER FISH); DISTRIBUTED BY: PFP LLC, Brooklyn, NY, 11211, USA; Product must be thoroughly cleaned and cooked before consumption.; PRODUCT OF VIETNAM; UPC: 6 946976 81
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Devices)·Z-1446-2026·2026-03-04

    Olympus resection sheath recalled due to ceramic tip breakage

    Olympus is recalling 207 units of its Resection Sheath, Model A22043T, after receiving complaints that the ceramic tip can break during use. The recall affects all lots distributed nationwide.

    Product
    Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide