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 the agency’s own highest classification or reported deaths or serious injuries, 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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3351–3375 of 39747

  • SevereFDA (Devices)·Z-1142-2025·2025-02-26

    Medical imaging device patient table mattress may cause patient falls

    Philips is recalling Allura Xper FD10 imaging devices because the patient table mattress may not securely hold patients during procedures, creating a fall hazard. The recall affects 2,274 units worldwide, including 459 in the U.S.

    Product
    Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0567-2025·2025-02-26

    ZAARAH HERBALS Shatavari Powder recalled for elevated lead contamination

    ZAARAH HERBALS brand Shatavari Powder is recalled due to elevated lead contamination at 6.50 mg/kg. The affected batch was distributed in NY, NJ, CT, and CA.

    Product
    ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine Powder 100g (3.5 oz); Manufactured by FALCON SYSTEM OF AYUREVEDIC PRODUCTS Auto Nagar, Belgaum, Karnataka 590015 (INDIA); Manufactured for: ZAARAH HERBALS, USA…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0245-2025·2025-02-26

    Fentanyl Transdermal Patches Recalled for Defective Delivery System

    Alvogen has recalled Fentanyl Transdermal System patches (25 mcg/h) nationwide due to a manufacturing defect where patches may be stacked together in a single pouch. Patients using affected lots should contact their healthcare provider.

    Product
    FENTANYL SYSTEM — FENTANYL SYSTEM (FENTANYL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1155-2025·2025-02-26

    Philips Azurion 5 M12 Patient Table Recalled for Fall Risk

    Philips Medical Systems is recalling Azurion 5 M12 imaging tables due to a mattress defect that could allow patients to fall from the table.

    Product
    Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1157-2025·2025-02-26

    Philips Azurion 7 B12 examination tables recalled due to patient fall risk

    Philips Medical Systems is recalling Azurion 7 B12 examination tables due to a mattress-related patient fall risk. The recall affects 602 total units, including 94 in the US and 508 internationally.

    Product
    Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1160-2025·2025-02-26

    Azurion 7 M20 Patient Tables Recalled for Patient Fall Risk

    Philips recalls Azurion 7 M20 patient tables due to a mattress defect that could cause patients to fall. Approximately 1,480 units in the US and 2,741 units overseas are affected.

    Product
    Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2025·2025-02-25

    L&V Food Supply Recalls Ineligible Frozen Dried Catfish Products

    L&V Food Supply is recalling approximately 1,152 pounds of peppered dried catfish imported from Vietnam because the source establishment is not eligible to export to the U.S.

    Product
    C&T Produce Wholesale Inc. Dba L&v Food Supply Recalls Ineligible Frozen, Dried Silurifomes Products Imported From Vietnam
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·25V116000·2025-02-24

    Mercedes-Benz Recalls S-Class Vehicles Due to Front Brake Hose Rupture Risk

    Mercedes-Benz is recalling 2021-2023 S-Class and Maybach vehicles because front brake hoses may rupture and leak fluid, increasing stopping distance and crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 500, S 500 4MATIC, S 580, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V115000·2025-02-24

    Kia EV9 rear drive unit motor shaft may be improperly welded

    Kia is recalling certain 2025 EV9 vehicles because the rear gear drive unit motor shaft may have been improperly welded and become damaged, causing a loss of drive power.

    Product
    KIA — KIA EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V114000·2025-02-21

    Spartan RV chassis fuel filter hose can separate causing leak and stall

    Shyft Group is recalling certain 2022-2025 Spartan RV Chassis K2 vehicles with Cummins L9 diesel engines because the remote fuel filter hose may separate from the fitting.

    Product
    SPARTAN — SPARTAN K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V109000·2025-02-21

    BMW X3 battery cable connection can overheat stalling the engine

    BMW is recalling certain 2025 X3 30 xDrive vehicles because the connection between the positive battery cable and the starter-generator may be improperly tightened and overheat.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25137·2025-02-20

    Electra E-Bikes Recalled Due to Crash Hazard From Loose Rear Fender

    Trek is recalling about 927 Electra e-bikes because the rear fender can come loose, contact the rear wheel, and stop the bike unexpectedly, posing a crash hazard. One injury with a fractured shinbone and meniscus tear has been reported.

    Product
    Electra E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25150·2025-02-20

    SuperATV Carrier Bearings for Polaris RZR Recalled for Fire and Burn Hazards

    SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S vehicles can allow the drive shaft to contact the fuel tank, causing fuel leaks and fire hazards. SuperATV is offering free replacement bearings to affected consumers.

    Product
    SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S Recreational Off Highway Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25138·2025-02-20

    Swagtron SG-5 Boost Electric Scooters Recalled for Fire and Burn Hazards

    Walmart recalls about 17,970 Swagtron SG-5 Boost electric scooters due to lithium-ion batteries that can overheat, smoke, and ignite, causing fire and burn hazards. One incident caused a burn injury and property damage to a residential building.

    Product
    Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V106000·2025-02-20

    BMW X3 rear door locks can be released with one motion

    BMW is recalling certain 2022-2024 X3 sDrive30i and xDrive30i vehicles because second-row door locking modules may allow the doors to be unlocked with a single motion, failing FMVSS 206.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0554-2025·2025-02-19

    Menma Ajitsuke Bamboo Shoots Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Menma Ajitsuke prepared bamboo shoots because the packaging is missing a "Keep Refrigerated" statement. The product requires refrigeration and improper storage could allow bacterial growth.

    Product
    Menma Ajitsuke prepared bamboo shoots; Product of Japan; Manufactured by: Choshiya Honten CO., LTD. Hamamatsu 431-1103 Japan UPC 4 923673 527332. Product is packaged in 8.8 OZ Plastic Pouches. 60 units per case.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0548-2025·2025-02-19

    Shirakiku Curvee Puffs Corn Puff Snack Recalled for Undeclared Milk Allergen

    Wismettac Asian Foods is recalling Shirakiku brand Curvee Puffs Corn Puff Snack because the product contains undeclared milk allergen. The affected product was distributed nationwide to approximately 471 consignees.

    Product
    Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK, Curry Flavor, NET WT 2.46 oz (70 g); Rear panel:Best Before YYYY.MM.DD; Nutritional Facts: 2.5 servings per container; Distributed by Wismettac Asian Foods, Inc.; 13409 Orden Drive, Santa Fe Spring, CA 90670; Product of…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1071-2025·2025-02-19

    Olympus Guide Sheath Kits recalled for potential radiopaque tip detachment

    Olympus Single Use Guide Sheath Kits (models K-201 through K-204) are recalled because the radiopaque tip of the guide sheath may detach and fall into the patient during respiratory procedures.

    Product
    Olympus Single Use Guide Sheath Kits with the following product descriptions and model numbers: 1. Single Use Guide Sheath Kit K-201 2.0MM Channel Set: Guide Sheath, Biopsy Forceps, Cytology Brush; Model Number: K-201 2. Single Use Guide Sheath Kit K-202 2.0MM Channel Set…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1116-2025·2025-02-19

    Wheelchair Speed Control Remote Recalled Due to Loss-of-Control Risk

    The Smart Drive MX2+ SpeedControl Dial remote is being recalled due to a faulty circuit board that could cause loss of control of the wheelchair power assist, potentially resulting in injury.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Food)·F-0553-2025·2025-02-19

    Pearl Milling Pancake & Waffle Mix Recalled for Undeclared Milk Allergen

    Frito-Lay is recalling Pearl Milling Company Original Pancake & Waffle Mix due to undeclared milk allergen. The product may cause allergic reactions in consumers with milk allergies.

    Product
    Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
    Category
    Food
    Distribution
    11 states