The Recall Desk

State

Delaware product recalls

73,218 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 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16401–16425 of 76656

  • SevereCPSC·23212·2023-06-01

    EGO Power+ Cordless Hedge Trimmers recalled for unexpected activation and laceration risk

    Chervon North America is recalling about 85,000 EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers due to a faulty rear trigger switch. The company has received 34 reports of unexpected activation, including 8 that caused lacerations requiring stitches.

    Product
    EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V391000·2023-06-01

    2023 Entegra Odyssey motorhomes recalled for loose rear axle bolts

    Jayco is recalling certain 2023 Entegra Odyssey motorhomes because bolts securing the rear axle rotor to the wheel hub may be improperly tightened, potentially causing wheel separation and increased crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA REDHAWK, GREYHAWK, ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V395000·2023-06-01

    Altec aerial device trucks: forward collision braking system software miscalibration

    Altec is recalling 2020-2023 aerial device trucks due to collision mitigation system software that may not be calibrated correctly, preventing the active braking system from activating. This increases the risk of a crash.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V394000·2023-06-01

    2022-2023 Land Rover Range Rover Rear Taillight Link Defect Recall

    Land Rover is recalling 2022-2023 Range Rovers because a damaged rear taillight link can cause exterior lights to fail, reducing visibility and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V392000·2023-06-01

    2023 Subaru Ascent Front Lower Control Arm Separation Recall

    2023 Subaru Ascent vehicles may have improperly tightened ball joint castle nuts in the lower control arm, risking separation and loss of vehicle control. Free replacement at dealers.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V390000·2023-06-01

    2020-2021 Jayco Melbourne Motorhomes Recalled for Instrument Cluster Failure

    Jayco is recalling certain 2020-2021 Melbourne motorhomes because the instrument cluster may fail and display nothing. Drivers would lose access to critical vehicle information, increasing crash risk.

    Product
    JAYCO — JAYCO MELBOURNE PRESTIGE, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23211·2023-06-01

    Jetson Nova and Star 3-Wheel Kick Scooters Recalled for Fall Hazard

    Jetson Electric Bikes is recalling about 15,300 Nova and Star 3-Wheel Kick Scooters because the rear wheel can loosen or fall off, posing a fall hazard to children. The company has received 12 reports of wheel loosening or falling, including one injury.

    Product
    Jetson Nova and Star 3-Wheel Kick Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1594-2023·2023-05-31

    COVID-19 At-Home Test Kits Recalled for Bacterial Buffer Contamination

    SD Biosensor is recalling 2,712,767 Pilot COVID-19 At-Home Test kits nationwide due to bacterial contamination in the liquid buffer component. Users may notice an odor from affected kits.

    Product
    Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V387000·2023-05-31

    Triple E Recalls 2023 Motorhomes Due to LPG Gas Leak Risk

    Triple E is recalling 2023 Unity and Wonder motorhomes because an improperly crimped 2-stage regulator may cause a gas leak, increasing the risk of fire.

    Product
    TRIPLE E RV — TRIPLE E RV, TRIPLE E WONDER, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V388000·2023-05-31

    Bugatti Recalls One 2023 Chiron Super Sport for Incorrect Wheels

    Bugatti is recalling one 2023 Chiron Super Sport because incorrect wheels were installed, which may cause loss of vehicle control in Top Speed Mode.

    Product
    BUGATTI — BUGATTI CHIRON SUPER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0755-2023·2023-05-31

    Injectable Drug Recalled for Unverified Sterility After FDA Inspection

    Central Admixture Pharmacy Services is recalling 1673 bags of HyperLyte CR Injection due to lack of sterility assurance. An FDA inspection raised questions about whether the product met sterility standards.

    Product
    HyperLyte CR Injection, 250 mL bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8094-2, code 7128580942.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0702-2023·2023-05-31

    OxyTOCIN-dextrose injectable recalled nationwide for sterility assurance concerns

    Central Admixture Pharmacy Services is recalling oxyTOCIN 20 units in dextrose 5%/Lactated Ringer's solution nationwide due to lack of sterility assurance identified during FDA inspection. 7,595 bags across multiple lot numbers are affected.

    Product
    oxyTOCIN 20 units added to dextrose 5%/Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6031-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0698-2023·2023-05-31

    FDA Recalls Neonatal Parenteral Nutrition Bags for Sterility Concerns

    Central Admixture Pharmacy Services recalled 328 neonatal parenteral nutrition bags nationwide due to FDA concerns about product sterility after an inspection.

    Product
    Neonatal PN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100 Allentown, PA 18106, NDC 71285-0429-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0693-2023·2023-05-31

    FDA Recalls Neonatal TPN Starter Bags for Sterility Concerns

    Central Admixture Pharmacy Services recalls 747 bags of Neonatal TPN Starter Bags due to FDA sterility concerns. Products were distributed nationwide across the USA.

    Product
    Neonatal TPN Starter Bag, Amino Acids (Trophamine) 4%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0422-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0664-2023·2023-05-31

    Cardioplegia Solution Recalled Due to Sterility Assurance Issues

    Central Admixture Pharmacy Services is recalling Cardioplegia Solution (Induction 4:1 High Potassium) due to lack of sterility assurance following an FDA inspection. The recall affects 84 bags distributed nationwide.

    Product
    Cardioplegia Solution, Induction 4:1 High Potassium, 30 mEq K, packaged in 415 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0106-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0930-2023·2023-05-31

    Geisha Medium Shrimp Recalled Due to Under-Processing Risk

    Kawasho Foods USA recalls Geisha Medium Shrimp (4 oz) due to potential under-processing. Do not consume; discard or return to point of purchase.

    Product
    Geisha Medium Shrimp; WT 4OZ(113g)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0725-2023·2023-05-31

    Vancomycin Sodium Chloride Injection Recalled Due to Sterility Assurance Concerns

    Central Admixture Pharmacy Services is recalling 11,338 bags of vancomycin sodium chloride injection nationwide due to FDA concerns about product sterility following an inspection.

    Product
    vancomycin added to 0.9% sodium chloride, 1.5 g/500 mL* (3 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6176-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0685-2023·2023-05-31

    Neonatal TPN Starter Bags Recalled for Sterility Assurance Issue

    Central Admixture Pharmacy Services recalls 138 bags of Neonatal TPN Starter Bag nationwide after FDA inspection questioned the products' sterility assurance. Affected lots expire between April and May 2023.

    Product
    Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with CALCIUM, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0407-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0707-2023·2023-05-31

    Injectable Oxytocin Lactated Ringer's Solution Recalled for Sterility Concerns

    Central Admixture Pharmacy Services is recalling 21,871 bags of injectable oxytocin mixed with Lactated Ringer's solution nationwide due to sterility assurance failures identified during an FDA inspection.

    Product
    oxyTOCIN 30 units added to Lactated Ringer's 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6039-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0716-2023·2023-05-31

    IV Potassium Phosphate Solution Recalled Due to Sterility Concerns

    Central Admixture Pharmacy Services recalls 9,432 bags of potassium phosphate injectable solution nationwide following FDA inspection findings that questioned the sterility of these pharmaceutical products.

    Product
    potassium phosphate 15 mmole added to 0.9% sodium chloride 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6060-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V366000·2023-05-31

    Marion Body Works Recalls 2022-2023 Spartan Fire Trucks for Transmission Defect

    Marion Body Works is recalling 2022 Spartan Fire Gladiator and 2023 Spartan Fire MetroStar emergency vehicles because the transmission control module may fail to engage 4th gear lockup, preventing the water pump from starting.

    Product
    MARION BODY WORKS — MARION BODY WORKS SPARTAN FIRE METROSTAR, SPARTAN FIRE GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0951-2023·2023-05-31

    TruBoost Drink Ruby Rev recalled for unapproved dietary ingredients

    TruVision Health LLC is recalling TruBoost Drink - Ruby Rev because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.

    Product
    TruBoost Drink - Ruby Rev
    Category
    Food
    Distribution
    50 states