The Recall Desk

State

Delaware product recalls

73,381 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
1,110
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 1,110 (32%) are Severe.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20876–20900 of 76819

  • HighNHTSA·22V519000·2022-07-21

    2022 Toyota RAV4 Air Bag Sensor May Deploy Incorrectly

    Toyota is recalling 2022 RAV4, RAV4 Hybrid, and RAV4 Prime vehicles because a front passenger seat occupant detection sensor may fail to properly detect occupants. This could cause improper air bag deployment during a crash, increasing injury risk.

    Product
    TOYOTA — TOYOTA RAV4 PRIME, RAV4 HYBRID, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V524000·2022-07-21

    2022 Jaguar XF, F-Type, F-Pace seat belt pretensioner failure

    Jaguar is recalling 2022 XF, F-Type, and F-Pace vehicles because the driver and front passenger seat belt pretensioners may be damaged, causing improper restraint during a crash.

    Product
    JAGUAR — JAGUAR F-TYPE, F-PACE, XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22186·2022-07-21

    Key West Knock Down Hammock Stands Recalled for Fall Hazard

    The Hammock Source is recalling about 32,500 Key West Knock Down Hammock Stands because the weld attaching the stand to the base can break, posing a fall hazard. Nine reports of stands breaking have been received, including two reports of scrapes and bruises.

    Product
    Key West Knock Down Hammock Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V527000·2022-07-21

    2022 Nissan Pathfinder rearview camera may fail due to software issue

    Nissan recalls 2022 Pathfinder rental vehicles where a software defect can disable the rearview camera, increasing crash risk. Affected customers will receive a free software update via dealer or over-the-air update.

    Product
    NISSAN — NISSAN TITAN, redundant ROGUE, FRONTIER, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V522000·2022-07-21

    2015-2021 Subaru WRX: Backup Light Switch Corrosion Recall

    Subaru recalls 2015-2021 WRX vehicles; backup light switch may corrode and fail, disabling backup lights and rearview camera in reverse, reducing visibility and increasing crash risk.

    Product
    SUBARU — SUBARU WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22759·2022-07-21

    Monti Kids Toy Box with Bins Recalled Due to Choking Hazard

    Monti Kids is recalling about 1,500 Toy Box with Bins units sold online from July 2021 through February 2022 because a small dowel can become exposed and detach, posing a choking hazard to young children.

    Product
    Monti Kids Toy Box with Bins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V526000·2022-07-21

    2022 Tesla Model S Front Bumper Defect May Cause Incorrect Airbag Deployment

    Tesla is recalling certain 2022 Model S vehicles because the front bumper carrier structure may alter crash detection, causing the front passenger airbag to deploy incorrectly during low speed crashes. This increases the risk of passenger injury.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V520000·2022-07-21

    2022-2023 Toyota Tacoma Defective Child Seat Anchor Welds

    Toyota is recalling certain 2022-2023 Tacoma vehicles due to insufficient welds in the upper child seat anchors. These defects may prevent proper anchoring of child seats, increasing the risk of injury during crashes or sudden stops.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22760·2022-07-21

    Vichy Laboratoires LiftActiv Peptide-C Ampoules Recalled for Laceration Hazard

    Vichy Laboratoires is recalling LiftActiv Peptide-C Anti-Aging Ampoules because the glass vials can break when opened, causing cuts to fingers and hands. The manufacturer has received 35 injury reports, including one requiring stitches.

    Product
    Vichy Laboratoires LiftActiv Peptide-C Anti-Aging Ampoules
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22187·2022-07-21

    Aqualung i330R SCUBA Diving Computers Recalled for Altitude Calculation Failure

    Aqualung i330R SCUBA diving computers can fail to adjust for user altitude and display incorrect dive-time calculations above 3,000 feet, creating risks of decompression sickness and drowning.

    Product
    Aqualung i330R SCUBA Diving Computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22761·2022-07-21

    Crye Precision LRB Leg Loops Recalled Due to Fall Hazard

    Crye Precision is recalling LRB Leg Loops because the buckle can loosen and slip when worn with a load-rated belt, creating a fall hazard. About 300 units are affected.

    Product
    Crye Precision LRB Leg Loops
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V521000·2022-07-21

    Cruiser Recalls 2022 Shadow Cruiser Travel Trailers Due to Incorrect Weight Label

    Cruiser RV is recalling 2022 Shadow Cruiser travel trailers because the federal certification label displays the incorrect Gross Axle Weight Rating, which may allow the vehicle to be overloaded.

    Product
    CRUISER RV — CRUISER RV SHADOW CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22188·2022-07-21

    Baby Mirror Activity Toys Recalled for Sharp Mirror Laceration Hazard

    Konges Sløjd Baby Mirror Activity Toys are being recalled because the mirror can detach from the silicone cover, exposing sharp edges that pose a laceration risk to children. About 85 units were sold in the United States.

    Product
    Baby Mirror Activity Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2022·2022-07-20

    Knorr Curry Chicken and Rice Soup Mix Recalled for Undeclared Milk

    MSI Express Inc. is recalling Knorr Curry Chicken and Rice Soup Mix because it contains undeclared milk, a known allergen.

    Product
    MSI Express Inc. Recalls Unilever Food Solutions U.S. Knorr Curry Chicken and Rice Soup Mix Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1428-2022·2022-07-20

    Natreve Vegan Protein Powder Recalled for Undeclared Milk Allergen

    Natreve Vegan Protein Powder (Lot# 46359 and 46360) is recalled nationwide due to an undeclared milk allergen.

    Product
    Natreve Vegan Protein Powder 10 servings, 13.1oz (371g), UPC 628831120003 18 servings, 1.47lbs/23.53oz (667g), UPC 628831110073
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1284-2022·2022-07-20

    Arti King tablets recalled for undeclared pharmaceutical ingredients

    Arti King Refozado con Ortiga y Omega 3 Tablets are recalled nationwide because FDA testing found undeclared diclofenac and dexamethasone. The product was marketed without FDA approval and should not be used.

    Product
    Arti King Refozado con Ortiga y Omega 3 Tablets, 100-count bottles, Hecho en Mexico por: "PLANTAS MEDICINALES DE MEXICO", Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800 Mexico, UPC 7 501031 111138
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1349-2022·2022-07-20

    CoolCurve+ Vacuum Applicator Recalled for Increased Paradoxical Hyperplasia Reports

    Zeltiq Aesthetics is voluntarily recalling CoolCurve+ ZELTIQ Vacuum Applicators due to increased reports of Paradoxical Hyperplasia during 2019–2021, an adverse event involving abnormal fat growth at treatment sites.

    Product
    CoolCurve+ ZELTIQ Vacuum Applicator REF BRZ-AP1-064-000
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Food)·F-1413-2022·2022-07-20

    Wawa Cold Brew Coffee Recalled for Undeclared Peanut Allergen

    Wawa cold brew coffee pints are being recalled due to undeclared peanuts. Approximately 1,000 units were distributed in Delaware, Florida, Maryland, New Jersey, Pennsylvania, Virginia, and Washington DC.

    Product
    Wawa COLD BREW COFFEE***ONE PINT (473ML)***MADE WITH WAWA COLD BREW***Nutrition Facts***INGREDIENTS: CREAM, SKIM MILK, LIQUID SUGAR (SUGAR, WATER), CORN SYRUP, WHEY, COFFEE, GUAR GUM, LOCUST BEAN GUM, TARA GUM, CARAMEL COLOR CONTAINS: MILK*DISTRIBUTED BY WAWA, INC, WAWA, PA…
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-1196-2022·2022-07-20

    BCAA Injection Vials Recalled for Lack of Sterility Assurance

    Tailor Made Compounding is recalling 180 vials of BCAA (branched-chain amino acid) injections nationwide due to inability to assure the product maintained sterility. Affected batches expire between April and June 2022.

    Product
    BCAAs (Leucine/Iso-Leucine/Valine) 10mg/10mg/5mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V516000·2022-07-20

    Audi Q8 and Q7 Fuel Pump Failure Risk Recall

    Volkswagen is recalling certain 2019-2021 Audi Q8 and 2020-2021 Audi Q7 vehicles due to a fuel pump component that may break, causing the pump to fail. A failed fuel pump can stall the engine, increasing crash risk.

    Product
    AUDI — AUDI Q8, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1197-2022·2022-07-20

    Biotin 5mg/mL injection recalled for lack of sterility assurance

    Tailor Made Compounding is recalling Biotin 5mg/mL injections distributed nationwide and in Puerto Rico because the manufacturer cannot assure the products were sterilized according to FDA standards.

    Product
    Biotin 5mg/mL, 5mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1195-2022·2022-07-20

    Ascorbic Acid Injectable Vials Recalled Due to Sterility Assurance Failure

    Tailor Made Compounding is recalling ascorbic acid injectable vials due to lack of sterility assurance. The affected vials were distributed nationwide and in Puerto Rico.

    Product
    Ascorbic Acid 500mg/mL, a) 25 ml-vial, b) 50 ml-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1239-2022·2022-07-20

    Testosterone Propionate Injectable Vials Recalled Over Sterility Assurance

    Testosterone propionate injectable vials are being recalled due to lack of assurance of sterility. The recall affects product distributed nationwide in the USA and Puerto Rico.

    Product
    Testosterone Propionate 100mg/ml, 10mL-vial, Room temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide