The Recall Desk

State

Delaware product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26926–26950 of 77004

  • ModerateFDA (Drugs)·D-0304-2021·2021-03-24

    Spironolactone Tablets Recalled Due to Potential Labeling Mix-Up

    Bryant Ranch Prepack is recalling 12 bottles of Spironolactone 50 mg tablets because they may contain 25 mg tablets due to a labeling error.

    Product
    Spironolactone Tablets, USP, 50 mg, packaged in 30-count bottles, Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA, NDC 63629-1067-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1249-2021·2021-03-24

    Medline Recalls RNA Medical Hemoglobin Control Product Due to Shipment Compromise

    Medline Industries is recalling 4 units of RNA Medical Hemoglobin Control product because the product was compromised during shipment. The recall affects distribution in Kentucky, Pennsylvania, and Ohio.

    Product
    RNA MEDICAL, QCHGB HEMOGLOBIN CONTROL, MULTI, REF QC HGB - Product Usage: monitoring the performance of Hemocue Hemoglobin Analyzers. It provides a convenient method of performing periodic QC checks to verify correct system measurement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0301-2021·2021-03-24

    Akorn Recalls Gabapentin Oral Solution Due to Impurity Specifications

    Akorn, Inc. is recalling Gabapentin Oral Solution because it failed impurity specifications during stability testing. The product was distributed nationwide.

    Product
    Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use Only, Rx only, Hi-Tech Pharmacal Co., Inc, Amityville, NY 11701, NDC Tray: 50383-311-07; NDC Unit Dose Cup 50383-311-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0308-2021·2021-03-24

    Breckenridge Recalls Omeprazole Capsules Due to Unknown Impurities

    Breckenridge Pharmaceutical is recalling 3,146 bottles of Omeprazole Delayed-Release Capsules, 20 mg, due to out-of-specification results for unknown impurities.

    Product
    Omeprazole Delayed-Release Capsules, USP, 20 mg, 1000 count bottles, Rx Only, distributed by Breckenridge Pharmaceutical, Inc., Berlin, CT, Manufactured by Tow Pharmaceutical Europe, S.L., Martorelles (Barcelona), Spain NDC 51991-643-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0306-2021·2021-03-24

    Edge Pharma Recalls Methacholine Challenge Test Kits Due to Storage Labeling Error

    Edge Pharma is recalling Methacholine Challenge 5-Syringe Test Kits because they were labeled with incorrect room temperature storage conditions instead of the required refrigerated conditions.

    Product
    Methacholine Challenge 5-Syringe Test Kits, Sterile Inhalation Solution, Preservative Free, 3 mL per syringe, Edge Pharma, LLC, 856 Hercules Dr., Dolchester, VT 06448 NDC # 05446-1600-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0309-2021·2021-03-24

    Teva Recalls Romidepsin Injection Vials Due to Impurity Failures

    Teva Pharmaceuticals is recalling 1,416 vials of Romidepsin Injection because stability testing revealed out-of-specification impurities.

    Product
    Romidepsin Injecton, 27.5 mg/5.5 mL (5 mg/mL) Rx Only, 5.5 ml vial, Teva Pharmaceuticals USA, Inc. NDC 0703-4004-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V198000·2021-03-22

    Audi Recalls A3 and S3 Models Due to Passenger Air Bag Defect

    Volkswagen Group of America is recalling specific Audi A3 and S3 models because the passenger air bag may deactivate while the seat is occupied.

    Product
    AUDI — AUDI S3, A3, A3 SPORTBACK E-TRON, RS 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2021·2021-03-20

    Avanza Pasta Recalls Beef and Poultry Products Lacking Federal Inspection

    Avanza Pasta, LLC is recalling approximately 9,847 pounds of beef and poultry ravioli and tortellini produced without federal inspection. No adverse reactions have been reported.

    Product
    Avanza Pasta, LLC Recalls Beef and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V194000·2021-03-19

    Isuzu and Chevrolet Trucks Recalled for Rear Axle U-Bolt Nut Defect

    Isuzu is recalling 2015-2021 Isuzu, Chevrolet, and International trucks because rear axle U-bolt nuts may loosen, causing axle misalignment and potential loss of power.

    Product
    CHEVROLET — CHEVROLET, INTERNATIONAL MOTORS, ISUZU 5500HD, 4500XD, CHEVY 5500HD, CHEVY 4500HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V197000·2021-03-19

    Mercedes-Benz Recalls Vehicles with Potential Front Roof Panel Bonding Defect

    Mercedes-Benz is recalling specific 2014-2020 models equipped with panoramic sunroofs because the front roof panel may not have been bonded correctly during a prior repair.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, S 450, C 350 E, CLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V196000·2021-03-19

    Mercedes-Benz Recalls 2006-2007 Models for Sunroof Glass Detachment Risk

    Mercedes-Benz is recalling 11,356 vehicles because the sunroof glass may detach, creating a road hazard and increasing crash risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ CLK500, C280, E500, C230
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-03192021-01·2021-03-19

    USDA Issues Public Health Alert for Uninspected Beef and Lamb Products

    USDA FSIS issued a public health alert for specific beef and lamb products from One Meat Corp. that were produced without federal inspection.

    Product
    FSIS Issues Public Health Alert for Beef and Lamb Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V189000·2021-03-18

    GM Recalls 2021 Chevrolet Express and GMC Savana for Fire Risk

    General Motors is recalling 2021 Chevrolet Express and GMC Savana vans with 6.6L engines because a battery cable defect may cause a short circuit and fire.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V191000·2021-03-18

    Arcimoto Recalls FUV and Deliverator Vehicles Due to Battery Shutdown Risk

    Arcimoto is recalling 2019-2020 FUV and 2020 Deliverator vehicles because high-voltage contactors may overheat, causing unexpected battery shutdowns and loss of motive power.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21098·2021-03-18

    HD Hudson Recalls illu-Mist Battery-Powered Garden Sprayers Due to Fire Hazard

    HD Hudson is recalling illu-Mist battery-powered garden sprayers because the lithium-ion battery can overheat and catch fire. Consumers should stop using the sprayers and contact the company for a replacement.

    Product
    illu-Mist Battery-Powered Garden Sprayers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V190000·2021-03-18

    Damaged Third-Row Seat Belts in 2021 GM Full-Size SUVs

    General Motors is recalling 2021 full-size SUVs because third-row seat belts may be entrapped or misrouted behind the seat-folding mechanism, potentially becoming damaged. A damaged seat belt could break during a crash, increasing the risk of occupant injury.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, SUBURBAN, ESCALADE ESV, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21730·2021-03-18

    Briggs & Stratton Recalls YTL Log Splitters Due to Engine Kickback Injury Hazard

    Briggs & Stratton is recalling YTL log splitters with 250cc engines due to a risk of engine kickback causing injury. Two incidents involving broken wrists have been reported.

    Product
    YTL Log Splitters with Briggs & Stratton 250cc engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V193000·2021-03-18

    2021 Tiffin Phaeton recreational vehicles recalled for loose valve stem

    Tiffin is recalling certain 2021 Phaeton recreational vehicles because the valve stem stabilizer can become loose, allowing the valve stem extender to contact the wheel, which can cause tire pressure loss and increase crash risk.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V188000·2021-03-18

    Chevrolet 2021 Camaro Axle Shaft Separation Defect Recall

    General Motors is recalling certain 2021 Chevrolet Camaro vehicles because the left or right axle shaft may be missing a retaining ring, which could separate during driving and cause loss of power, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1209-2021·2021-03-17

    RTI Surgical Recalls CervAlign Anterior Cervical Plate System Due to Locking Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 20mm Material Number: 66-120 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide