The Recall Desk

State

Delaware product recalls

73,503 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
2026-10-14

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.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25101–25125 of 76941

  • ModerateFDA (Drugs)·D-0728-2021·2021-08-25

    Avicel Microcrystalline Cellulose Recall for Out-of-Specification Conductivity

    DuPont Nutrition USA, Inc. is recalling Avicel microcrystalline cellulose (bulk PH101 NF, PH102 NF, PH200 NF) due to out-of-specification conductivity results. The product was distributed nationwide and internationally.

    Product
    Avicel, Mirocrystalline cellulose, packaged in bulk as PH101 NF, PH102 NF, PH200 NF, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0726-2021·2021-08-25

    Gavilyte-C Oral Solution Recalled for Failed Stability Specification

    Novel Laboratories/Lupin Pharmaceuticals is recalling Gavilyte-C (polyethylene glycol-3350 and electrolytes with flavor pack) due to failed stability testing and out-of-specification osmolarity. The product is distributed nationwide.

    Product
    GAVILYTE - C — GAVILYTE - C (POLYETHYLENE GLYCOL-3350 AND ELECTROLYTES WITH FLAVOR PACK)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0727-2021·2021-08-25

    Cholestene Capsules Recalled for Marketing Without Approved Application

    High Performance Formulas is recalling Cholestene capsules (red yeast rice supplement, 1200 mg per 2 capsules, 120-count bottles) because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).

    Product
    Cholestene capsules, 1200 mg of red yeast rice per 2 capsules, 120-count bottle, Manufactured by: High Performance Formulas, L.L.C. (HPF, L.L.C.) P.O. Box 1311, Morrisville, PA 19067, UPC 640485-10093-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0724-2021·2021-08-25

    Combipatch Transdermal System Recalled for Failed Stability Specifications

    Noven Pharmaceuticals is recalling Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg per day because certain lots failed stability specifications and tested out of specification for shear.

    Product
    COMBIPATCH (ESTRADIOL/NORETHINDRONE ACETATE TRANSDERMAL SYSTEM) — COMBIPATCH (ESTRADIOL/NORETHINDRONE ACETATE TRANSDERMAL SYSTEM) (ESTRADIOL/NORETHINDRONE ACETATE TRANSDERMAL SYSTEM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0751-2021·2021-08-25

    Econazole Nitrate Cream 1% recalled due to labeling mispack

    Teligent Pharma is recalling Econazole Nitrate Cream 1% in 85-gram bulk tubes due to incorrect labeling. The product was distributed nationwide.

    Product
    Econazole Nitrate Cream 1%, 85 grams bulk shippers, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-022-85 ; packaged in tubes.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0729-2021·2021-08-25

    Acetaminophen 325 mg tablets recalled for discoloration and cGMP deviations

    Spirit Pharmaceuticals is recalling Acetaminophen 325 mg Regular Strength Pain Reliever tablets due to discoloration and current good manufacturing practice (cGMP) deviations. The recall affects one lot distributed nationwide.

    Product
    Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0752-2021·2021-08-25

    Triamcinolone Acetonide Ointment Mispack Recall by Teligent Pharma

    Teligent Pharma is recalling Triamcinolone Acetonide Ointment USP 0.1% due to a labeling mispack affecting Lot #16630 with expiration 03/2023. The recall was issued due to incorrect labeling on the product.

    Product
    Triamcinolone Acetonide Ointment USP, 0.1% 80 g cartons, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-014-80 ; packaged in tubes.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·21188·2021-08-25

    Wee Gallery wooden tray puzzles recalled for choking hazard

    Wee Gallery is recalling Ocean and Safari animal wooden tray puzzles because the octopus and elephant puzzle pieces can break, posing a choking hazard to young children.

    Product
    Ocean and Safari animal wooden tray puzzles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V657000·2021-08-24

    PL Custom Emergency Vehicles Recall Rear Brake Line Wear Issue

    PL Custom is recalling 2019 Dodge RAM 5500 emergency vehicles because rear brake lines may wear, risking brake loss and crashes.

    Product
    PL CUSTOM — PL CUSTOM TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V656000·2021-08-24

    Crane Carrier Recalls 2020-2021 LET2 Trucks for Fuel Hose Leak Risk

    Crane Carrier is recalling 94 LET2 vehicles from 2020-2021 because a fuel hose may leak, increasing the risk of fire if exposed to an ignition source.

    Product
    CRANE CARRIER — CRANE CARRIER, CRANE LET2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21C003000·2021-08-24

    Dorel Maxi-Cosi Pria 85 Child Seat Recall for Tether Anchor Defect

    Dorel is recalling Maxi-Cosi Pria 85 convertible child seats because they may not adequately protect children from head injury if installed with only a lap belt.

    Product
    CHILD SEAT:VEHICLE TETHER ANCHOR recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V655000·2021-08-23

    Reitnouer Recalls 2017-2019 Trailers Due to Steering Arm Detachment Risk

    Reitnouer is recalling 2017-2019 Steer Axle trailers because the steering arm may detach, potentially causing loss of control or road hazards.

    Product
    REITNOUER TRAILERS — REITNOUER TRAILERS REITNOUER TRAILERS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V654000·2021-08-23

    PL Custom Recalls 2021 Ford E-450 Emergency Vehicle for LCD Defect

    PL Custom is recalling one 2021 Ford E-450 emergency vehicle because its LCD display may freeze or fail, potentially delaying emergency efforts.

    Product
    PL CUSTOM — PL CUSTOM TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V652000·2021-08-23

    2021 Ford Explorer and Lincoln Aviator side air bag assembly defect

    Ford and Lincoln are recalling certain 2021 Explorer and Aviator vehicles. Side air bag attachment weld studs may detach during deployment, potentially failing to provide proper protection in a crash.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V649000·2021-08-20

    Chevrolet Malibu and Cadillac XT4 seat belt fastener defects

    General Motors is recalling certain 2016-2021 Chevrolet Malibu and 2019-2021 Cadillac XT4 vehicles because rear seat belt retractors may be improperly secured with loose or missing fasteners, potentially affecting safety in a crash.

    Product
    CADILLAC — CADILLAC, CHEVROLET XT4, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V650000·2021-08-20

    Chevrolet Bolt EV battery fire hazard recall for defective modules

    General Motors is recalling 2020-2022 Chevrolet Bolt EV and 2022 Bolt EUV vehicles. The high-voltage battery could catch fire when charged to full or nearly full capacity, increasing risk of injury.

    Product
    CHEVROLET — CHEVROLET BOLT EUV, BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V651000·2021-08-20

    2022 Volkswagen Taos Fuel Supply Connector Detachment Recall

    Volkswagen is recalling certain 2022 Taos vehicles because the underhood fuel supply quick-connector may detach from the fuel line, creating fuel leaks that increase risks of engine stalling and fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V648000·2021-08-19

    Peterbilt 2021-2022 Commercial Trucks Recalled for Brake System Clearance Defect

    PACCAR is recalling certain 2021-2022 Peterbilt commercial trucks due to insufficient clearance in the Hill Start Assist valve assembly, which may damage the rear brake hose and disable rear braking. Dealers will inspect and repair the assembly free of charge.

    Product
    PETERBILT — PETERBILT 389, 567, 367, 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21776·2021-08-19

    John Deere Compact Utility Tractors Recalled for Wheel Detachment Risk

    Deere & Company is recalling approximately 200 John Deere compact utility tractors (models 4044M, 4044R, 4052M, 4052R, 4066M, 4066R) because rear wheel spacer bolts can be improperly torqued during manufacturing, causing the wheel to fall off and the tractor to overturn.

    Product
    John Deere compact utility tractors
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21775·2021-08-19

    Infant Bath Seats Recalled Due to Drowning Hazard

    Frieyss infant bath seats fail to meet federal safety standards and can tip over while in use, posing a drowning hazard to babies. About 120 units were sold exclusively online at Amazon.com from March through April 2021.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2193-2021·2021-08-18

    HeartWare HVAD Driveline Extension Cable Recalled for Cardiac Safety Concerns

    Medtronic is recalling the HeartWare HVAD Driveline Extension Cable (443 units) due to higher frequency of neurological adverse events and mortality in clinical comparisons with other heart assist devices. The pump may experience restart delays or failures.

    Product
    HeartWare HVAD Driveline Extension Cable, REF 100US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2197-2021·2021-08-18

    Heartware HVAD Pump Accessories Recalled Over Increased Mortality and Device Failures

    Heartware is recalling HVAD Pump Accessories due to clinical data showing higher rates of neurological adverse events and mortality compared to other left ventricular assist devices, and reports of pump malfunctions.

    Product
    HeartWare HVAD Pump Accessories, REF MCS1753AK
    Category
    Medical Device
    Distribution
    Distributed nationwide