The Recall Desk

State

Delaware product recalls

73,187 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total
3,438
Critical
477
Severe
939
Most recent
2026-09-23

Of the 3,438 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 939 (27%) are Severe.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13501–13525 of 76625

  • 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
  • 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 PUMPER, RPM, AERIAL, RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V032000·2024-01-19

    Maxi-Metal Recalls 2020-2023 Kenworth and Freightliner Trucks for Fire Risk

    Maxi-Metal is recalling 2020-2023 Kenworth and Freightliner trucks because a firmware defect in certain electrical nodes may prevent circuits from shutting off, increasing the risk of fire.

    Product
    MAXI-METAL — MAXI-METAL KENWORTH, FREIGHTLINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V029000·2024-01-19

    2024 Forest River IBEX trailers recalled for suspension fastener safety

    Forest River is recalling certain 2022–2024 IBEX, NO BOUNDARIES, and R-POD trailers because fasteners for the independent suspension may loosen and allow the suspension to detach, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER NO BOUNDARIES, IBEX, R-POD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V030000·2024-01-19

    Forest River Recalls 2024 Shasta Oasis Trailers for Lighting Defect

    Forest River is recalling 2024 Shasta Oasis travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers.

    Product
    SHASTA — SHASTA OASIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V033000·2024-01-19

    Nova Bus Recalls 2017-2019 LFS Models for Door Window Marking Defect

    Nova Bus is recalling 2017-2019 LFS and LFS Artic buses because driver's door windows may have incorrect DOT code marks, potentially leading to improper glass replacement and reduced visibility.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide