The Recall Desk

State

Delaware product recalls

73,597 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
475
Severe
1,112
Most recent
2026-10-14

Of the 3,438 recalls naming Delaware we have scored against our rubric, 475 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,112 (32%) are Severe.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29476–29500 of 77035

  • HighCPSC·20162·2020-08-12

    Intertex Recalls B-Air, BlueDri, and Soleaire Blowers Due to Fire Hazard

    Intertex is recalling approximately 189,000 B-Air, BlueDri, BlueDri Pro, and Soleaire blowers because unprotected side outlets pose a fire hazard.

    Product
    B-Air, BlueDri, BlueDri Pro and Soleaire Blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2753-2020·2020-08-12

    Randox Lipase Assay Substrate Recalled for Imprecision in Quality Control

    Randox Laboratories is recalling specific batches of Lipase R2 Substrate due to confirmed imprecision in quality control and patient samples.

    Product
    Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2749-2020·2020-08-12

    Teleflex Pleur-Evac Chest Drainage Devices Recalled for Packaging Compromise

    Teleflex Medical Inc. is recalling Pleur-Evac chest drainage devices because sterile packaging may be compromised, potentially affecting sterility.

    Product
    Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2747-2020·2020-08-12

    Siemens DCA Vantage Barcode Scanner Recalled for Data Integrity Issues

    Siemens Healthcare is recalling 1,800 DCA Vantage Handheld Barcode Scanners because they may fail to verify check digits or incorrectly process barcodes, potentially leading to data errors.

    Product
    DCA Vantage Handheld Barcode Scanner - Zebra Model - Model # DS4308 - HC0015BZZWW external accessory to DCA Vantage Analyzer US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2752-2020·2020-08-12

    Randox Lipase Assay Buffer Recalled for Imprecision in Quality Control

    Randox Laboratories is recalling specific batches of Lipase Colorimetric R1 Buffer due to confirmed imprecision in quality control and patient samples.

    Product
    Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1487-2020·2020-08-12

    Vilvet Pharmaceuticals Recalls VILAMIT MB Due to cGMP Deviations

    Vilvet Pharmaceuticals is recalling 11,640 bottles of VILAMIT MB capsules due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and nationwide.

    Product
    VILAMIT MB (118 mg methenamine, 36 mg phenyl salicylate, 40.8 mg sodium phosphate monobasic, 10.0 mg methylene blue and 0.12 mg hyoscyamine sulfate), Rx Only, 100 Capsules per Bottle, Manufactured for: Vilvet Pharmaceuticals Inc., Chester Springs, PA 18425, NDC 71186-002-35.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2751-2020·2020-08-12

    Randox Lipase Assay Reagent Recalled for Imprecision in Quality Control and Patient Samples

    Randox Laboratories is recalling specific batches of Lipase Colorimetric Reagent due to confirmed imprecision in quality control and patient samples.

    Product
    Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2744-2020·2020-08-12

    Sutter Swyng Non-Stick Bipolar Forceps Recalled for Incorrect Package Insert Labeling

    Sutter Medizintechnik GmbH is recalling 1,337 units of Sutter Swyng non-stick bipolar forceps because the package insert incorrectly displays the Ethylene Oxide sterilization symbol instead of the irradiation symbol.

    Product
    Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps are provided with bayonet-style handle design with straight or angled tips and different total lengths. They are to be connected through an appropriate bipolar…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1488-2020·2020-08-12

    Vilvet Pharmaceuticals Recalls VILEVEV MB Urinary Antiseptic Due to cGMP Deviations

    Vilvet Pharmaceuticals is voluntarily recalling 1,716 bottles of VILEVEV MB Urinary Antiseptic due to current Good Manufacturing Practice (cGMP) deviations.

    Product
    VILEVEV MB Urinary Antispetic (81.0 mg methenamine, 40.8 mg sodium phosphate monobasic and 10.8 mg methylene blue, 0.12 mg hyoscyamine sulfate and 32.4 mg phenyl salicylate), Rx Only, 90 Tablets per Bottle, Manufactured for: Vilvet Pharmaceuticals, Inc., Chester Springs, PA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1143-2020·2020-08-12

    Vitamin Shoppe Recalls Calcium Citrate Plus Magnesium & Vitamin D Supplements

    Vitamin Shoppe is recalling specific bottles of Calcium Citrate Plus Magnesium & Vitamin D because sample analysis revealed the product is sub-potent for Vitamin D.

    Product
    The Vitamin Shoppe Calcium Citrate Plus Magnesium & Vitamin D. 100 count (VS-1086; UPC:6653601086), 300 count (VS-1087; UPC: 6653601087), and 600 count (VS-1123; UPC: 6653601123).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V472000·2020-08-11

    Triumph Recalls 2019-2020 Motorcycles Due to Wiring Harness Defect

    Triumph is recalling 2019-2020 Street Scrambler and Street Twin motorcycles because a misrouted wiring harness may contact the frame, causing the engine to stall and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH STREET SCRAMBLER, STREET TWIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V471000·2020-08-10

    BMW Recalls Motorcycles Due to Fuel Pump Flange Crack Risk

    BMW is recalling specific motorcycles because a fuel pump flange may crack, causing a fuel leak that increases fire risk.

    Product
    BMW — BMW K1200 GT, HP2 SPORT, K1200 S, K1200 R SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2020·2020-08-10

    Mr. Wok Foods Recalls Meat and Poultry for Undeclared Allergens

    Mr. Wok Foods is recalling approximately 242,640 pounds of frozen meat and poultry products due to misbranding and undeclared allergens.

    Product
    Mr Wok Foods Inc. dba Maxfield Foods — Mr. Wok Foods, Inc. Recalls Multiple Meat and Poultry Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V470000·2020-08-10

    Ford Recalls 2020 Lincoln Corsair for Rear Coil Spring Clearance Issue

    Ford is recalling 2,965 2020 Lincoln Corsair vehicles because rear coil springs may lack sufficient clearance, potentially breaking and affecting vehicle handling.

    Product
    LINCOLN — LINCOLN CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20T015000·2020-08-10

    Linglong Americas Recalls Venezia Crusade HT Tires Due to Sidewall Separation

    Linglong Americas Inc. is recalling specific Venezia Crusade HT tires because they may experience lower sidewall separation, which can lead to sudden tire failure and increase the risk of a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V467000·2020-08-10

    Ford Recalls 2020 F-150 Trucks Due to Starter Motor Fire Risk

    Ford is recalling 2020 F-150 vehicles because an incorrect attachment nut on the starter motor may cause electrical arcing and increase the risk of a fire.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E054000·2020-08-10

    Kiel Recalls Avance Passenger Seats Due to Seat Belt Defect

    Kiel is recalling specific Avance passenger seats for motorcoaches because the seat belt retractors may not function properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V468000·2020-08-10

    Entegra Qwest motorhome wiring defect may cause airbag malfunction

    Jayco is recalling 2020-2021 Entegra Qwest motorhomes and related Jayco models because front seat wiring harnesses may be routed incorrectly, creating a risk of unexpected or failed airbag deployment.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE PRESTIGE, QWEST, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V464000·2020-08-07

    Mercedes-Benz Recalls 2020 GLE 450 for Windshield Bonding Defect

    Mercedes-Benz is recalling one 2020 GLE 450 because the windshield may not be bonded correctly, which could reduce the effectiveness of the passenger air bag in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V463000·2020-08-07

    American Hauler Recalls 2018 Trailers Due to Axle Weld Failures

    American Hauler is recalling 2018 Air-Lite, Arrow, Falcon/XC, and Night Hawk trailers because spindle weld failures on the axles may increase the risk of a crash or injury.

    Product
    AMERICAN HAULER — AMERICAN HAULER FALCON/XC, ARROW, NIGHT HAWK, AIR-LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V466000·2020-08-07

    2017-2021 Freightliner Business Class M2 trucks recalled for electrical harness defect

    Daimler Trucks North America is recalling certain 2017-2021 Freightliner Business Class M2 trucks because the engine harness may contact and chafe, potentially short-circuiting and causing engine stall during operation.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V465000·2020-08-07

    BMW Recalls 2020 X5 and X7 Models Due to Starter Motor Bolt Risk

    BMW is recalling 21 vehicles because an extra bolt in the starter motor could fall into the transmission, causing an engine stall and increasing crash risk.

    Product
    BMW — BMW X7, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V461000·2020-08-06

    GM Recalls 2020 Chevrolet Corvette for Front Trunk Release Defect

    General Motors is recalling 2020 Chevrolet Corvette vehicles because the front trunk release button may fail to function after the vehicle is shut off for ten minutes, potentially trapping a person inside.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide