The Recall Desk

State

Delaware product recalls

73,576 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.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27976–28000 of 77014

  • ModerateFDA (Devices)·Z-0635-2021·2020-12-23

    Helena Laboratories Recalls K-ACT Actalyke Clotting Test Tubes

    Helena Laboratories is recalling K-ACT Actalyke Clotting Test Tubes due to complaints of cracked or split caps.

    Product
    K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0169-2021·2020-12-23

    Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures

    Hikma Pharmaceuticals is recalling 1.3 million vials of Sodium Chloride Injection USP 0.9% because pH test results were out of specification.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0615-2021·2020-12-23

    Medline Recalls RevMedX Trauma Dressings Due to Package Seal Integrity Issues

    Medline Industries is recalling RevMedX Trauma Dressings because of package seal integrity issues. The recall affects 15,780 units distributed in the US and several international countries.

    Product
    RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per Case; Sterile - Product Usage: are intended to absorb exudates.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0612-2021·2020-12-23

    Medtronic Percept PC Neurostimulator Recall Due to Software Connection Failure

    Medtronic is recalling 12 Percept PC Implantable Neurostimulators because a software anomaly in the A620 Patient Programmer prevents connection to the device.

    Product
    Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0180-2021·2020-12-23

    Fusion Health Recalls Pharmorigins Core Supplement for Unapproved Additive

    Fusion Health and Vitality LLC is recalling Pharmorigins Core dietary supplements due to the unapproved use of a food additive and unapproved marketing statements.

    Product
    PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0159-2021·2020-12-23

    Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity

    Taro Pharmaceuticals is recalling specific lots of Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal Cream, NET WT 1 oz (30 g), Distributed by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10531. Made in Canada. UPC 3 51672 20022 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0570-2021·2020-12-23

    Zimmer Biomet Recalls Polaris Spinal System Screws for Labeling Update

    Zimmer Biomet is updating instructions for Polaris and Cypher spinal screws to warn against using them with direct current stimulation due to construct failure risks.

    Product
    Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0158-2021·2020-12-23

    Taro Recalls TopCare Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling TopCare Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    TOPCARE — TOPCARE (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0154-2021·2020-12-23

    Taro Recalls Kroger Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling Kroger Athlete's Foot Cream because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    KROGER — KROGER (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0146-2021·2020-12-23

    Zydus Recalls Lansoprazole Tablets for Failed Dissolution Specifications

    Zydus Pharmaceuticals is recalling 22,848 cartons of Lansoprazole 30 mg tablets nationwide because they failed to meet dissolution specifications.

    Product
    LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0151-2021·2020-12-23

    Taro Recalls Clotrimazole Cream Due to Unknown Impurity

    Taro Pharmaceuticals is recalling Equate Athlete's Foot cream because an unknown impurity was detected above specification limits.

    Product
    CLOTRIMAZOLE — CLOTRIMAZOLE (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0148-2021·2020-12-23

    Biogen Recalls Vumerity Capsules Due to Dissolution Test Failures

    Biogen is recalling 5,307 bottles of Vumerity capsules because they failed dissolution testing. The medication may not release the drug as intended.

    Product
    VUMERITY — VUMERITY (DIROXIMEL FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0153-2021·2020-12-23

    Taro Recalls Kaiser Permanente Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling specific lots of Kaiser Permanente Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    Kaiser Permanente Clotrimazole Cream USP, 1% Antifungal Cream, NET WT 1 oz (28.4 g), Manufactured by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T1C1 Distributed by Kaiser Foundation Hospitals Livemore, CA 94551-9756. Made in Canada. NDC 0179-8014-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V808000·2020-12-22

    GM Recalls 2020 Chevrolet Bolt EV for Brake Caliper Fracture Risk

    General Motors is recalling 2020 Chevrolet Bolt EV vehicles because a front left brake caliper may fracture, potentially reducing brake performance and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V809000·2020-12-22

    Escape Trailer Recalls 2020 RVs Due to Gas Leak Risk

    Escape Trailer is recalling 2020 RV trailers because a stove component may cause a gas leak, increasing the risk of fire.

    Product
    ESCAPE — ESCAPE ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21715·2020-12-22

    2021 Can-Am Outlander and Renegade ATVs Recalled for Rear Wheel Separation

    Bombardier Recreational Products is recalling 2021 Can-Am Outlander and Renegade ATVs because a rear wheel can separate, causing a crash hazard.

    Product
    2021 Can-Am Outlander and Renegade All-Terrain Vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V764000·2020-12-21

    GM Recalls 2010-2013 Buick and Chevrolet Models for Rear Suspension Defect

    General Motors is recalling specific Buick and Chevrolet vehicles because excessive corrosion protection on rear toe links may cause them to fracture, increasing crash risk.

    Product
    BUICK — BUICK, CHEVROLET LACROSSE, REGAL, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V802000·2020-12-21

    Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Brake Fluid Leak

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because rear brake calipers may leak fluid, allowing air into the hydraulic brake system.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V804000·2020-12-21

    Thor Motor Coach Recalls 2018-2019 Hurricane and Windsport Motorhomes

    Thor Motor Coach is recalling 2018-2019 Hurricane and Windsport motorhomes because overhead cabinets may detach and fall on occupants.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V807000·2020-12-21

    2021 FCCC Trucks Recalled: Brake Caliper Tie Bar Fasteners May Be Loose

    DTNA recalls certain 2021-2022 commercial trucks with potentially loose or missing brake caliper tie bar fasteners, which could affect brake function and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC, THOMAS BUILT BUSES BUSINESS CLASS M2, MC, MBC, MT55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E092000·2020-12-21

    Bendix Brake Light Switch Recall Due to Potential Jamming

    Bendix is recalling specific brake light pressure switches that may leak air, causing electrical contacts to jam and brake lights to malfunction.

    Product
    EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V803000·2020-12-21

    Volvo Bus Recalls 2015-2020 9700 Models for Transmission Hub Failure

    Volvo Bus is recalling 2015-2020 9700 buses because a transmission hub may fail, potentially disabling the vehicle and forcing passengers to transfer on the roadside.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V805000·2020-12-21

    SVI Trucks Recalls 2020 Fire Rescue Trucks Due to Display Lockup

    SVI Trucks is recalling 2020 Fire Rescue Trucks because the instrument cluster display may lock up, potentially delaying emergency efforts and increasing injury risk.

    Product
    SVI TRUCKS — SVI TRUCKS SVI TRUCKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V806000·2020-12-21

    2022 Thomas Built Buses Brake Tie Bar Installation Defect Recall

    Daimler Trucks recalls 278 model year 2022 Thomas Built SAF-T-Liner C2 school buses due to improper brake tie bar installation. The defect could increase crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·030-2020·2020-12-19

    Nestlé Recalls Lean Cuisine Baked Chicken Meals Due to Plastic Contamination

    Nestlé Prepared Foods is recalling Lean Cuisine Baked Chicken meal products that may contain pieces of hard white plastic. No illnesses have been reported.

    Product
    Nestlé Prepared Foods Recalls Lean Cuisine Baked Chicken Meal Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide