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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2301–2325 of 36523

  • SevereUSDA FSIS·021-2025-EXP·2025-06-25

    Starway Recalls Ineligible Frozen Siluriformes Fish Products Imported from Vietnam

    Starway International Group is expanding a recall for frozen fish products from an ineligible Vietnamese establishment. No adverse reactions have been reported.

    Product
    Starway International Group LLC Expands Recall for Ineligible Frozen Siluriformes Fish Products Imported from Vietnam
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0046-2025·2025-06-25

    Lancaster LF Authentic Greek Salad Kit Recalled for Salmonella Risk

    Reser's Fine Foods is recalling Lancaster LF Authentic Greek Salad Kits distributed in MA and PA because the cucumbers may be contaminated with Salmonella. The kits are implicated in an ongoing Salmonella outbreak.

    Product
    Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This is wholesale kit consisting of pre-packaged components in a corrugated box for assembly by retail delis. Kit contains sealed bags of cut produce (sliced cucum
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·25V414000·2025-06-25

    International CV brake pressure sensor can leak fluid causing fire

    International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0053-2025·2025-06-25

    Vegetable Bowls and Trays Recalled for Potential Salmonella Contamination

    GBC Food Services is recalling vegetable bowls and vegetable ranch trays due to potential Salmonella contamination. Affected products were purchased between May 8 and May 21, 2025.

    Product
    Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Bowl $10 26 oz 860010507131 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Ranch Tray No Dip Small 19.50 oz 850054894335 Purchase Dates: 05/08/2025 to 05/21/2025 Large Vegetable Tray
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0493-2025·2025-06-25

    UMOVY ACIDO HIALURONICO supplement recalled for undeclared prescription drugs

    UMOVY ACIDO HIALURONICO dietary supplement has been recalled because it contains undeclared prescription ingredients Dexamethasone and Diclofenac. The product was marketed without FDA approval.

    Product
    UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0056-2025·2025-06-25

    Cucumber Carrot Ranch Pack 20oz recalled for Salmonella contamination

    GBC Food Services is recalling Cucumber Carrot Ranch Pack 20oz due to potential Salmonella contamination. The affected products were purchased between May 8 and May 21, 2025, and distributed across nine states.

    Product
    Cucumber Carrot Ranch Pack 20oz 850065403557 Purchase Dates: 05/08/2025 to 05/21/2025
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0492-2025·2025-06-25

    UNAVY ACIDO HIALURONICO supplement recalled for undeclared pharmaceutical ingredients

    UNAVY ACIDO HIALURONICO hyaluronic acid supplement is being recalled because it contains three undeclared pharmaceutical ingredients: Dexamethasone, Diclofenac, and Omeprazole. The product was marketed without FDA approval and poses health risks from the unlisted drugs.

    Product
    UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1902-2025·2025-06-25

    Cook Beacon Tip Angiographic Catheters Recalled for Tip Separation Risk

    Cook Incorporated is recalling specific lots of Beacon Tip 5.0 Fr Angiographic catheters due to the risk that the catheter tip may separate during use. The affected catheters were distributed worldwide.

    Product
    Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lengths and tip curves and some catheters are manufactured with a hydrophilic coati
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·25V380000·2025-06-23

    GEM Recalls 2022-2025 Electric Vehicles Due to Ball Joint Separation Risk

    GEM is recalling 2022-2025 e2, e4, e6, and eLXD vehicles because improperly tightened fasteners may cause the front lower ball joint to separate, potentially leading to a loss of steering control.

    Product
    GEM — GEM E4, E6, ELXD, E2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V425000·2025-06-20

    Travel trailer patio door transit latch cannot be opened from inside

    Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V422000·2025-06-19

    Honda Recalls 2013 Accord Vehicles for Driveshaft Corrosion Risk

    Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.

    Product
    HONDA — HONDA ACCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V419000·2025-06-19

    Subaru Forester child seat anchor bolts may come loose

    Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V385000·2025-06-19

    Vanguard Recalls 2021-2023 VXP Trailers Due to Hook Box Defect

    Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.

    Product
    VANGUARD — VANGUARD VXP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0033-2025·2025-06-18

    Jean's Classy Fresh Salsa Hot recalled due to Salmonella contamination

    TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Hot (6/12 oz. plastic tubes) due to Salmonella contamination. The affected product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Salsa, Hot 6/12 oz., Plastic tube, 6 per case .
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-1869-2025·2025-06-18

    Blood Products Administration Set Filter Mis-Assembly Recall

    Fresenius Kabi USA is recalling IVENIX INFUSION SYSTEM LVP Blood Products Administration Sets due to a mis-assembly error that may prevent the drip chamber filter from properly filtering large blood particulates.

    Product
    IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter, 15 mL. Intravascular Administration Set.
    Category
    Medical Device
    Distribution
    18 states
  • SevereNHTSA·25V413000·2025-06-18

    Mazda CX-50 airbag module software may cause improper deployment

    Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.

    Product
    MAZDA — MAZDA CX-50 HYBRID, CX-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25351·2025-06-18

    MaxKare Electric Blankets Recalled for Burn and Fire Hazards

    MaxKare electric blankets (model HB18A) sold on Walmart.com can overheat and catch fire, posing burn hazards. Yumo has received 34 reports of overheating, including 3 burn injuries and 2 fires.

    Product
    MaxKare Electric Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1934-2025·2025-06-18

    Philips Intera 1.5T MRI Systems Gradient Coil Fire Risk Recall

    Philips is recalling Intera 1.5T Omni/Stellar MRI systems due to a gradient coil component failure that can produce smoke and fire, risking patient and operator injury or death.

    Product
    Intera 1.5T Omni/Stellar; Product Number: 781104;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0022-2025·2025-06-18

    Sysco Corporation Egg Salad Sandwich Recalled for Salmonella Risk

    Sysco Corporation is recalling egg salad sandwiches (HKSAN169, 1/5.76 oz) because cucumbers used in the product may be contaminated with Salmonella.

    Product
    HKSAN169 1/5.76OZ CREATED FRESH Sub- Egg Salad on Everything Ficelle ALL LOT CODES HKSAN169 1/5.76 OZ. EA Crested Fresh Sub- Egg Salad on Everything Ficelle ALL LOT CODES
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Devices)·Z-1935-2025·2025-06-18

    Philips Intera Achieva 1.5T Pulsar MRI Systems Gradient Coil Fire Risk

    Philips is recalling certain Intera Achieva 1.5T Pulsar MRI systems due to a potential component failure in the gradient coil that could generate smoke and/or fire, risking patient and operator injury or death.

    Product
    Intera Achieva 1.5T Pulsar; Product Number: 781171;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1953-2025·2025-06-18

    Tecfen Medical 20G MVR Sideport Knife ophthalmic sterility recall

    Tecfen Medical is recalling its 20G (1.2mm) MVR Sideport Knife Straight (Model QKN2312) ophthalmic knives due to sterility assurance concerns. The recall affects 38 units distributed in the US and internationally.

    Product
    Brand Name: Tecfen Medical Product Name: 20G (1.2mm) MVR Sideport Knife Straight Model/Catalog Number: QKN2312 Software Version: No software Product Description: This is an ophthalmic knife (manual( that is to be sterile and packaged individually in Tyvek 1059B. MVR sideport
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1952-2025·2025-06-18

    Tecfen Medical 2.8mm Slit Knife Angled Sterility Assurance Recall

    Tecfen Medical is recalling 2.8mm Slit Knife, Angled (Model QKN2808) ophthalmic surgical instruments due to sterility assurance concerns. Affected units were distributed in the US and internationally.

    Product
    Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife, Angled Model/Catalog Number: QKN2808 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25342·2025-06-18

    AstroAI 4-Liter/6-Can Minifridges Recalled Due to Fire and Burn Hazards

    AstroAI is recalling approximately 249,100 minifridges because the electrical switch can short circuit, causing fires and burn hazards. At least 70 incidents of smoking, burning, melting, or fire have been reported, including two fires that caused more than $360,000 in property damage.

    Product
    4 Liter/6 Can Minifridges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25345·2025-06-18

    TADAKAZU Baby Loungers Recalled for Suffocation Fall and Entrapment Hazards

    TADAKAZU Baby Loungers violate federal infant sleep product standards, posing risks of suffocation, falls, and entrapment. The CPSC recommends immediate discontinuation and contact with TADAKAZU for refund.

    Product
    TADAKAZU Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide