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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18676–18700 of 114351

  • HighFDA (Drugs)·D-0253-2024·2024-01-24

    Secret anti-perspirant spray recalled for potential benzene contamination

    The FDA is recalling Secret powder fresh anti-perspirant spray due to potential benzene contamination found at the manufacturing facility.

    Product
    SECRET ANTIPERSPIRANT — SECRET ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0237-2024·2024-01-24

    Ibuprofen and Famotidine Tablets Recalled for Foreign Tablet Contamination

    Ascend Laboratories is recalling 3,288 bottles of Ibuprofen and Famotidine tablets nationwide because a stray Rasagiline Mesylate tablet was discovered in an unopened bottle during quality control.

    Product
    IBUPROFEN AND FAMOTIDINE — IBUPROFEN AND FAMOTIDINE (IBUPROFEN AND FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0729-2024·2024-01-24

    Ultrasound examination tables recalled for backrest platform stress fractures

    Oakworks recalled 20 Ultrasound EA and G3 examination tables due to backrest platform stress fractures that prevent proper operation in inclined positions. Affected units are identified by serial number.

    Product
    Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Supports [left & right}
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0760-2024·2024-01-24

    Maquet Rolite OR Light Systems Recall Due to Fall Risk

    Getinge USA is recalling 236,793 Maquet Rolite operating room light systems due to a potential for the light fixture to fall. No injuries have been reported.

    Product
    Maquet Rolite OR Light Systems, Model Numbers and Catalog Numbers ROL PWDII50SF - ARDPWT309001A, ROL PWDII50SF - ARDPWT309002A, ROL PWDII50SF - ARDPWT309009A, ROL PWDII50SF - ARDPWT309010A, ROL PWDII70SF - ARDPWT309007A, ROL PWDII70SF - ARDPWT309008A, ROL PWDII70SF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0748-2024·2024-01-24

    SOLTIVE SuperPulsed Laser Fibers Recalled for Potential Fiber Breakage During Surgery

    Olympus is recalling 82,200 units of SOLTIVE SuperPulsed Laser Fibers due to instruction inconsistencies that could cause fiber breakage during use, potentially resulting in burns or foreign material in the patient.

    Product
    SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S, TFL-FBX200S, TFL-FBX365S, TFL-FBX550S, TFL-FBX940S, TFL-FBX150BS, TFL-FBX200BS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0252-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled Due to Potential Benzene Contamination

    Procter & Gamble is recalling Old Spice SWEAT DEFENSE ULTIMATE CAPTAIN anti-perspirant spray due to potential benzene contamination at the manufacturing facility. Affected products have expiration dates through September 2023.

    Product
    Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum Chlorohydrate 23.5%, Anti-Perspirant, Topical spray can 3.8 OZ (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-385-10, UPC 0 37000 74947 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2024·2024-01-24

    Maquet Hanaulux HLX3000 Operating Room Light Systems Recall for Fall Hazard

    Getinge Usa Sales Inc is recalling approximately 236,793 Maquet Hanaulux HLX3000 operating room light systems nationwide and globally due to a potential for the light system to fall in the operating room.

    Product
    Maquet Hanaulux HLX3000 OR Light Systems, Model Numbers and Catalog Numbers H3 BC - HM567811111C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V039000·2024-01-24

    2024 Rolls-Royce Spectre Recalled for Electrical Ground Cable Defect

    BMW is recalling 2024 Rolls-Royce Spectre vehicles because adhesive residue on the ground cable may cause electrical issues, increasing fire and shock risks.

    Product
    ROLLS-ROYCE — ROLLS-ROYCE SPECTRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0756-2024·2024-01-24

    Cardinal Health Suction Canister Liners may lose suction due to misalignment

    Cardinal Health Medi-Vac suction canister liners in specific lots may lose suction on low settings due to misalignment of the liner with the outer canister. Stop using affected units and contact the manufacturer for replacements.

    Product
    Cardinal Health Suction Canister Liner, MEDI-VAC CRD 1000 mL Suction Canister Liner Kit with 6 mm 1.8 m Tube, REF 65651-517
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0230-2024·2024-01-24

    Freskaro Magnesium Citrate oral solution recalled for bacterial contamination

    Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor) nationwide due to the presence of Acetobacter nitrogenifigens bacteria.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0722-2024·2024-01-24

    Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling 439,240 cases of chicken broth products sold under multiple brands for potential microbial contamination. Products were distributed across 37 states.

    Product
    Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken Broth, UPC: 50428430095, carton H-E-B, 48oz Chicken Broth, UPC: 41220610013, carton HEB Select Ingredients, 32oz Chicken Broth, UPC: 41220610006, 41220610075…
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-0736-2024·2024-01-24

    BD PosiFlush Prefilled Saline Syringes Recalled for Incorrect Stopper

    Becton Dickinson is recalling 5,085,120 BD PosiFlush Prefilled Saline Syringes due to an incorrect stopper that increases injection force and may trigger pump alarms.

    Product
    PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0726-2024·2024-01-24

    Organic Chicken Broth Recalled Nationwide for Potential Microbial Contamination

    TreeHouse Foods is recalling multiple brands of organic chicken broth due to potential microbial contamination. Approximately 439,240 cases were distributed across 37 states.

    Product
    Organic Chicken Broth sold under: 365 Organic, 32oz Chicken Broth, Good & Gather, 32oz Organic Chicken Broth Sprouts, 32oz Organic Chicken Broth Natures Promise, 32oz Organic Chicken Stock Market Basket, 32oz Organic Chicken Stock O Organics, 32oz Organic Chicken Broth
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Food)·F-0732-2024·2024-01-24

    Central Market Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods recalls Central Market 32oz Organic No Salt Added Chicken Broth (lot code 98C06193) for potential microbial contamination affecting 439,240 cases distributed across 41 states.

    Product
    Central Market 32oz Organic No Salt Added Chicken Broth
    Category
    Food
    Distribution
    37 states
  • LowFDA (Devices)·Z-0737-2024·2024-01-24

    V. Mueller Bandage Scissors recalled for pink dye staining on handles

    Steris Corporation is recalling V. Mueller Universal Bandage Scissors (Model SU2014-001) due to an incorrect resin carrier in the handle cover. Pink dye residue may appear on scissors and sterilization pouches after processing.

    Product
    V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through tape and bandages Model: SU2014-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V036000·2024-01-23

    Tiffin motorhome driver seat pedestal plates may be improperly welded

    Tiffin is recalling certain 2022 motorhomes because the pedestal mounting plate on the driver's seat may be improperly welded, allowing the seat assembly to loosen or detach. 507 units affected.

    Product
    TIFFIN — TIFFIN ALLEGRO RED 360, ALLEGRO BUS, ZEPHYR, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V038000·2024-01-23

    Suzuki Recalls 2024 GSX1300R Motorcycles Due to Brake Fluid Leak Risk

    Suzuki is recalling 2024 GSX1300R motorcycles because an incorrectly tightened brake fluid pipe flare nut may cause a leak, reducing braking performance and increasing crash risk.

    Product
    SUZUKI — SUZUKI GSX1300R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V037000·2024-01-23

    Brinkley Model Z axle spindle welds may fail and detach wheels

    Brinkley RV is recalling certain 2024 Model Z recreational vehicles because the axle spindle weld may fail, resulting in the wheel assembly detaching from the axle. 17 units affected.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V028000·2024-01-19

    Marion Fire Apparatus Recalled for Electrical Wiring Fire Risk

    Marion Body Works is recalling 2020-2022 fire apparatus vehicles due to a firmware defect that can cause electrical circuits to overheat and increase fire risk.

    Product
    MARION — MARION RPM, AERIAL, PUMPER, RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide