The Recall Desk

State

Delaware product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19426–19450 of 76804

  • HighFDA (Devices)·Z-0166-2023·2022-11-09

    Medline CVC Barrier Kit Recalled for Breached Pouch Seals

    Medline is recalling CVC barrier kits (Lot 22ABT774) due to breather pouches with seal openings that could compromise sterility of the surgical kit contents.

    Product
    MEDLINE CVC BARRIER KIT, REF DYNJ80485. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0165-2023·2022-11-09

    Medline Radiology Procedure Pack Breather Pouches Recalled for Seal Defects

    Medline is recalling 240 Radiology Procedure Packs because some breather pouches show seal openings that could compromise sterility. The affected kits were distributed nationwide.

    Product
    MEDLINE RADIOLOGY PROCEDURE PACK, REF DYNJ67150A. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0152-2023·2022-11-09

    Implantable Defibrillator Software Error Causes Inaccurate Battery Display

    Boston Scientific's EMBLEM MRI S-ICD implantable defibrillators contain a software defect with an incorrect manufacturing date that causes inaccurate battery capacity display. The recall affects 142 devices distributed worldwide.

    Product
    EMBLEM MRI S-ICD, Subcutaneous Implantable Defibrillator, Model A219, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0162-2023·2022-11-09

    Medline Lithotomy Sterile Surgical Kit Recalled for Compromised Breather Pouch Seal

    Medline is recalling 96 sterile surgical kits (REF DYNJ50099C, Lot 22DBL482) distributed nationwide due to complaints of openings in breather pouches that compromise sterility and increase contamination risk.

    Product
    MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0105-2023·2022-11-09

    Bella Cucina Pizza Mix Recalled for Undeclared Wheat Allergen

    Bella Cucina Tradizionale Pizza and Foccacia Mix is being recalled because the label does not declare wheat, a common allergen. Consumers with wheat allergies could experience allergic reactions.

    Product
    Bella Cucina Artful Food Tradizionale Pizza and Foccacia Mix Net Wt. 15 oz 422g can, Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
    Category
    Food
    Distribution
    45 states
  • HighFDA (Food)·F-0098-2023·2022-11-09

    Bella Cucina Fresh Basil Pesto Recalled for Undisclosed Milk Allergen

    Bella Cucina Artful Food is recalling Fresh Basil Pesto because the label does not disclose milk. The product may cause allergic reactions in consumers with milk allergies.

    Product
    Bella Cucina Artful Food Fresh Basil Pesto Net Wt. 3 oz (84.5g) bag, UPC 6 19193 00211 3 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
    Category
    Food
    Distribution
    45 states
  • HighFDA (Food)·F-0100-2023·2022-11-09

    Bella Cucina Spinach Artichoke Bruschetta Spread Recalled for Undisclosed Milk

    Bella Cucina Artful Food is recalling Spinach Artichoke Bruschetta Spread because the label does not indicate milk. Consumers with milk allergies should not consume this product.

    Product
    Bella Cucina Artful Food Spinach Artichoke Bruschetta Spread Net Wt. 10 oz (286g) jar, UPC 6 19193 00501 5 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
    Category
    Food
    Distribution
    45 states
  • HighFDA (Devices)·Z-0147-2023·2022-11-09

    Fogarty Biliary Balloon Probes recalled for latex deterioration

    Edwards Lifesciences is recalling Fogarty Biliary Balloon Probes due to confirmed latex deterioration in pouches. The recall affects 26,560 units distributed worldwide.

    Product
    Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0168-2023·2022-11-09

    Pediatric Vision Scanner Battery Pack Poses Fire Risk

    Rebiscan is recalling Blinq Pediatric Vision Scanners (Model BQ830) because the battery pack may vent and catch fire if a cell voltage drops below 2.5V.

    Product
    Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0025-2023·2022-11-09

    Ranibizumab eye implant recalled for non-functioning delivery system

    Genentech is recalling Susvimo ocular implants (452 units nationwide) due to manufacturing defects in the drug delivery system. A few patients have experienced non-functioning implants.

    Product
    SUSVIMO — SUSVIMO (RANIBIZUMAB)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0173-2023·2022-11-09

    BD Multitest 6-Color TBNK tubes recalled for partial label detachment

    BD Multitest 6-Color TBNK tubes are being recalled due to partial label detachment. The defect can cause tubes to stick together or lead to automation errors when used with the flow cytometer's automated loader.

    Product
    BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995), for use with BD FACSLyric, BD FACSCanto II, and BD FACSCanto flow cytometers to determine the percentages and absolute counts of human lymphocyte subsets in peripheral whole blood for immunophenotyping.
    Category
    Medical Device
    Distribution
    43 states
  • HighNHTSA·22V828000·2022-11-04

    Forest River Recalls 2022-2023 East to West Alta Travel Trailers

    Forest River is recalling 2022-2023 East to West Alta travel trailers because side marker lights may not reflect light as intended, reducing visibility.

    Product
    EAST TO WEST — EAST TO WEST ALTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23034·2022-11-03

    BLACK+DECKER Garment Steamers Recalled for Burn Hazard from Hot Water

    Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23032·2022-11-03

    FUUL Lamp Oil Recalled for Non-Child-Resistant Packaging and Labeling Failures

    FHS Retail is recalling about 1,700 units of FUUL 1.9L Pure Liquid Paraffin Lamp Oil because the packaging is not child-resistant and the label omits mandatory safety information required by federal law. The product can cause fatal chemical pneumonia or lung damage if ingested.

    Product
    FUUL 1.9L Pure Liquid Paraffin Lamp Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V825000·2022-11-03

    2021-2022 Ford Bronco Rearview Camera Display May Distract Drivers

    Ford is recalling 2021-2022 Bronco vehicles with rearview camera systems because the camera image may remain displayed after the vehicle shifts out of reverse, potentially distracting drivers and increasing crash risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23035·2022-11-03

    AirWick Fresh New Day Aerosol Air Fresheners Recalled for Rupture and Laceration Risk

    Reckitt is recalling about 67,000 AirWick Fresh New Day aerosol air fresheners in Fresh Linen and Fresh Waters scents due to a missing corrosion inhibitor in one batch that can cause cans to rupture or leak. No injuries have been reported.

    Product
    AirWick Fresh New Day® aerosol air fresheners - "Fresh Linen" and "Fresh Waters" scents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23036·2022-11-03

    Clarks Women's Navy Canvas Shoes Recalled for Chemical Hazard

    Clarks Americas is recalling three styles of women's navy canvas shoes sold from February to October 2022 because prolonged contact with the shoe material can expose wearers to toxic chemicals benzidine and/or dimethoxybenzidine.

    Product
    Breeze Ave, Breeze Shore and Breeze Step women's shoes in navy colors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V827000·2022-11-03

    2021 Cadillac Escalade daytime running lights control software defect

    General Motors is recalling 2021 Cadillac Escalade vehicles. The daytime running lights may not deactivate when headlights are on, which may cause glare and reduce visibility, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23707·2022-11-03

    BS Interactive Stashables Finger Skateboard Ramp Sets Lead Paint Hazard

    BS Interactive is recalling Stashables Finger Skateboard Ramp Sets because the miniature skateboards and scooters contain lead paint levels exceeding federal limits and fail lead content bans, posing a lead poisoning risk to young children.

    Product
    Stashables Finger Skateboard Ramp Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23708·2022-11-03

    Myx Connected Exercise Bicycles Recalled for Pedal Detachment Risk

    Myx is recalling approximately 162,000 MYX I, MYX II, and MYX II Plus exercise bicycles because pedals can loosen or detach during use, causing injury. Myx has received 864 reports of pedal loosening or detachment, including 75 injury reports involving bruises and cuts.

    Product
    MYX I, MYX II and MYX II Plus Connected Exercise Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23031·2022-11-03

    Bolt Foldable Children's Scooters Recalled for Excessive Lead Paint

    Anker Play Products is recalling about 5,000 Bolt Foldable Children's Scooters sold at discount stores from March through May 2022. The paint contains lead levels exceeding the federal ban, creating a lead poisoning hazard for young children.

    Product
    Bolt Foldable Children's Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide