The Recall Desk

State

Delaware product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25301–25325 of 76947

  • HighFDA (Devices)·Z-2184-2021·2021-08-11

    Abbott Alinity c Reagent Kit Recall Due to Potential Test Result Errors

    Abbott Laboratories is recalling its Alinity c Activated Alanine Aminotransferase reagent kit due to potential analytical errors that could produce incorrect test results. The issue affects certain lot numbers distributed worldwide.

    Product
    REF: 08P1820, Abbott Alinity c Activated Alanine Aminotransferase reagent Kit, Alinity c Activated Alanine Aminotransferase Reagent Kit,, IVD, CE, UDI: (01) 00380740132569
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0835-2021·2021-08-11

    Stop n Shop Mini Muffin Blueberry Streusel Recall for Listeria

    Stop n Shop 12ct Mini Muffin Blueberry Streusel (12 oz) is being recalled nationwide due to potential Listeria monocytogenes contamination. The product was distributed to retailers across the country.

    Product
    Stop n Shop 12ct Mini Muffin Blueberry Streusel - 12 oz.; UPC: 216055 003990
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2186-2021·2021-08-11

    Abbott Activated Alanine Aminotransferase Reagent Accuracy Issue Recall

    Abbott's A-ALT laboratory reagent may produce inaccurate results in samples with very high enzyme levels or elevated bilirubin, potentially affecting patient diagnoses. The affected product (REF 8L92-21) was distributed worldwide.

    Product
    REF 8L92-21, Abbott Activated Alanine Aminotransferase, for use with Architect, IVD, CE, UDI: (01) 00380740017866
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21177·2021-08-11

    Delayed Egress Locks Recalled Due to Entrapment Risk

    dormakaba USA is recalling about 2,400 Delayed Egress Locks (model DE8310) that may fail to open, trapping occupants and preventing emergency evacuation. The firm has received 56 incident reports, with no injuries reported.

    Product
    Delayed Egress Locks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0826-2021·2021-08-11

    Great Value Blueberry Snack Muffins Recalled for Listeria Contamination Risk

    Great Value Blueberry Snack Muffins (12 oz, UPC 078742-201207) are being recalled nationwide because they may be contaminated with Listeria monocytogenes. Consumers should not eat the affected product.

    Product
    Great Value Blueberry Snack Muffins - 12oz, 8 per case; UPC: 078742-20120 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0836-2021·2021-08-11

    Freshness Guaranteed Mini Muffins Recalled for Listeria Risk

    Freshness Guaranteed Blueberry Streusel and Strawberry Streusel Mini Muffins are being recalled nationwide due to possible Listeria monocytogenes contamination. Consumers should not eat the product and should discard or return it.

    Product
    Freshness Guaranteed Blueberry Streusel/Strawberry Streusel Mini Muffins - 12 oz., 10 per case; UPC: 078742-32200 1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0906-2021·2021-08-11

    Frozen Cooked Shrimp Recall Due to Potential Salmonella Contamination

    Avanti Frozen Foods is recalling multiple brands of frozen cooked, peeled, and deveined shrimp due to potential Salmonella contamination. The affected products were distributed nationally through importers and distributors.

    Product
    Cooked, Peeled and Deveined, Tail-on, Shrimp. CENSEA, Frozen Cooked, peeled and deveined, Tail Off Shrimps IQF 2 LB Printed Polythene Pouch CHICKEN OF THE SEA, Frozen Cooked, peeled and deveined, Tail On Shrimps IQF with Cocktail Sauce 16oz Printed Polythene Trays HONEST…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0842-2021·2021-08-11

    The Worthy Crumb Blueberry Streusel Muffins Recalled for Listeria Risk

    The Worthy Crumb Assorted Large Muffins in Blueberry Streusel flavor may be contaminated with Listeria monocytogenes. The affected product was distributed nationwide and should not be consumed.

    Product
    The Worthy Crumb Assorted Large Muffins - Blueberry Streusel - 3.6oz; UPC: 7 70981-49136 3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0699-2021·2021-08-11

    Pfizer Chantix Tablets Recalled for N-nitroso-varenicline Impurity

    Pfizer is recalling Chantix (varenicline tartrate) 0.5mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit. The recall affects 59,232 bottles.

    Product
    CHANTIX — CHANTIX (VARENICLINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0701-2021·2021-08-11

    Pfizer Chantix Tablets Recalled for Nitroso Impurity Above FDA Limit

    Pfizer is recalling Chantix (varenicline tartrate) 1 mg tablets nationwide because certain lots contain the impurity N-nitroso-varenicline above FDA's acceptable interim intake limit due to manufacturing deviations.

    Product
    CHANTIX — CHANTIX (VARENICLINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2172-2021·2021-08-11

    GlideScope Go Video Monitors Recalled for Waterproof Rating Defect

    Verathon recalls GlideScope Go Monitors due to failure to meet IP67 waterproof rating, which may allow fluid ingress and loss of functionality.

    Product
    GlideScope Go Monitors
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Devices)·Z-2202-2021·2021-08-11

    Beta-Hydroxybutyrate diagnostic reagent recalled due to stability degradation

    Stanbio Laboratory is recalling Cardinal Health Beta-Hydroxybutyrate in vitro diagnostic reagents due to reagent instability causing out-of-range quality control values that may affect diagnostic accuracy.

    Product
    Cardinal Health Beta-Hydroxybutyrate . in vitro diagnostic reagent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2173-2021·2021-08-11

    Amia Automated PD System User Guide Incorrectly Describes Ultrafiltration Limit Function

    Baxter's user guide for the Amia Automated PD System incorrectly describes how the Ultrafiltration Limit setting controls the Extra Last Drain Mode. This documentation error could affect patients' ability to properly end therapy sessions.

    Product
    Sharesource Connectivity Platform for Use with the Amia Automated PD System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0700-2021·2021-08-11

    Pfizer Chantix Tablets Recalled for N-Nitroso-Varenicline Impurity

    Pfizer is recalling approximately 350,985 cartons of Chantix (varenicline tartrate) tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit. The recall affects multiple lot numbers with expiration dates ranging from September 2021 to January 2023.

    Product
    CHANTIX — CHANTIX (VARENICLINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2199-2021·2021-08-11

    Diagnostic Reagent Stability Issues Lead to Out-of-Range Quality Control Values

    Stanbio Laboratory is recalling Beta-Hydroxybutyrate LiquiColor diagnostic reagent due to reagent deterioration that causes lower than expected or out-of-range quality control values, affecting test accuracy.

    Product
    Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2203-2021·2021-08-11

    In Vitro Diagnostic Reagent Recalled Due to Stability Deterioration

    Cardinal Health Beta-Hydroxybutyrate diagnostic reagent has been recalled due to stability deterioration causing out-of-range quality control values. No illnesses have been reported.

    Product
    Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in vitro diagnostic reagent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2200-2021·2021-08-11

    Beta-Hydroxybutyrate Diagnostic Reagent Recalled for Stability Degradation

    Stanbio Laboratory recalled Beta-Hydroxybutyrate Reagent A due to deterioration in reagent stability. The degradation resulted in out-of-range Quality Control values that could affect diagnostic accuracy.

    Product
    Beta-Hydroxybutyrate Reagent A - Enzyme (unlabeled). in vitro diagnostic reagent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2021·2021-08-10

    Serenade Foods Recalls Frozen Raw Breaded Stuffed Chicken Products

    Serenade Foods is recalling approximately 59,251 pounds of frozen, raw, breaded stuffed chicken products due to possible Salmonella Enteritidis contamination.

    Product
    Serenade Foods, Division of Maple Leaf Farms, Inc. — Serenade Foods Recalls Frozen Raw Breaded Stuffed Chicken Products due to Possible Salmonella Enteritidis Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V629000·2021-08-10

    2020-2021 Polaris Slingshot vehicles recalled for loose rear wheel studs

    Polaris is recalling certain 2020-2021 Slingshot vehicles because rear wheel studs may not have been fully pressed into the axle, risking wheel detachment and crashes. Dealers will inspect and replace the affected parts free of charge.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V623000·2021-08-10

    Starcraft Allstar XL Buses Recalled for Fuel Heater Fire Risk

    Forest River is recalling 2017-2018 Starcraft Allstar XL buses because the fuel heater may overheat, melt, and catch fire or cause engine stalling.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V625000·2021-08-10

    2021 Lincoln Corsair fuel delivery module leak recall

    Ford is recalling 2021 Lincoln Corsair vehicles due to a fuel delivery module that may leak, causing low fuel pressure and engine stall, which increases the risk of a crash.

    Product
    FORD — FORD, LINCOLN ESCAPE, CORSAIR, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V627000·2021-08-10

    Husqvarna 701 Motorcycles Recalled for Rear Axle Nut Risk

    KTM is recalling 2018-2020 Husqvarna Vitpilen 701 and 2019-2020 Svartpilen 701 motorcycles because a loose rear axle nut could cause the license plate to hit the wheel.

    Product
    HUSQVARNA — HUSQVARNA VITPILEN 701, SVARTPILEN 701
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V628000·2021-08-10

    Custom Fire Spartan Emergency Vehicles Recalled for Pump Solenoid Defect

    Custom Fire is recalling 2009-2021 Spartan emergency vehicles because a corroded solenoid may cause loss of water pressure, increasing injury risk.

    Product
    CUSTOM FIRE — CUSTOM FIRE SPARTAN GLADIATOR, SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V626000·2021-08-10

    Cottrell Recalls 2019-2021 1-Car Trailers for Missing Reflectors

    Cottrell is recalling 2019-2021 1-Car Carrier trailers because they lack required side and rear reflex reflectors, which may reduce visibility and increase crash risk.

    Product
    COTTRELL — COTTRELL 1-CAR
    Category
    Vehicle
    Distribution
    Distributed nationwide