The Recall Desk

State

Delaware product recalls

73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27526–27550 of 77008

  • HighFDA (Devices)·Z-0917-2021·2021-02-03

    Philips Respironics V680 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 3,453 V680 ventilators worldwide because the navigation ring may fail or cause erratic parameter changes.

    Product
    Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 3,213 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.

    Product
    Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0908-2021·2021-02-03

    Philips Respironics V60 Ventilator Recall for Navigation Ring Issues

    Respironics is recalling 3,752 V60 Ventilators worldwide due to potential navigation ring malfunctions that may cause erratic parameter changes or inoperability.

    Product
    Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2020·2021-02-03

    Philips Telemetry Transceiver Recall for Heart Rate Display Failure

    Philips is recalling 21,672 telemetry transceivers because they may fail to display heart rates or generate alarms when used with specific Patient Information Center software.

    Product
    TRx4851A 2.4 GHz IntelliVue Tele TRX, Model Number 862231; Includes Service Numbers 453564052401, 453564052411, 453564052441, 453564052451, 453564166851, 453564166861
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0918-2021·2021-02-03

    Fujifilm Synapse PACS Software Recalled for Clinical Reporting Errors

    Fujifilm Medical Systems is recalling Synapse PACS Software versions 7.0.0 and 7.0.1 because the software fails to update measurements when ventricular traces are changed by different users.

    Product
    FUJIFILM Synapse PACS Software: versions 7.0.0 and 7.0.1 - Product Usage: intended for use as a web based application on an off-the shelf PC which meets or exceeds minimum specifications and is networked with a FUJIFILM Synapse PACS server.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0242-2021·2021-02-03

    Good & Gather Four Cheese Gnocchi Recalled for Foreign Material

    EMILIA FOODS SRL is recalling Good & Gather Four Cheese Gnocchi because the product may contain foreign material.

    Product
    Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Keep Frozen. Needs to be Fully Cooked. UPC 0 85239-10366 1 Product of Italy. Dist by Target Corporation, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0930-2021·2021-02-03

    B. Braun Introcan IV Safety Catheters Recalled for Lack of FDA Approval

    Braxton Medical Corporation is recalling B. Braun Introcan IV Safety Catheters because the products do not have FDA approval for sale in the United States.

    Product
    B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood intravascular.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0865-2021·2021-02-03

    Nihon Kohden PSG-1100 Sleep Diagnostic System Recalled for Electrical Safety Non-Conformance

    Nihon Kohden America Inc is recalling 189 PSG-1100 Sleep Diagnostic Systems because they do not meet the IEC 60601-1 electrical safety standard.

    Product
    PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI (01) 04931921108383; Made in Japan The PSG-1100 Sleep Diagnostic System is a digital PSG amplifier intended to record the electrical activity of the brain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0932-2021·2021-02-03

    Fujifilm Recalls Wako HDL-C/LDL-C Calibrator Due to Labeling Error

    Fujifilm is recalling Wako HDL-C/LDL-C Calibrator Lot EL629 because incorrect concentration values were printed on the bottle labels, which may result in incorrect testing results.

    Product
    Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used with Wako L-Type HDL-C or L-Type LDL-C for the determination of high density lipoprotein cholesterol (HDL-C) or low density lipoprotein cholesterol (LDL-C) in serum or plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0727-2021·2021-02-03

    Philips ProxiDiagnost N90 X-ray System Recalled for Software Lock-in Defect

    Philips is recalling 91 ProxiDiagnost N90 X-ray systems because kV and mA values may not lock correctly after a command, potentially affecting image quality.

    Product
    ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0931-2021·2021-02-03

    Yukon polyaxial screw component recalled for incorrect laser marking

    The Yukon polyaxial screw component in the Yukon Spinal System was recalled because it was incorrectly laser marked with wrong dimensions.

    Product
    Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026), component of YUKON Spinal System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0243-2021·2021-02-03

    Bausch Health Recalls Mephyton Tablets Due to Impurity D Failure

    Bausch Health is recalling 895 bottles of Mephyton (phytonadione) 5mg tablets because Impurity D failed stability testing specifications.

    Product
    Mephyton (phytonadione) Tablets 5mg, 100-count bottle, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC Bridgewater, NJ 08807 USA NDC 0187-1704-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0244-2021·2021-02-03

    Bausch Health Recalls Phytonadione Tablets Due to Impurity D

    Bausch Health is recalling Phytonadione Tablets 5mg because Impurity D exceeded specifications during stability testing. The recall covers 14,089 bottles distributed nationwide.

    Product
    Phytonadione Tablets 5mg, 30-count bottle, Rx Only, Manufactured For: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA NDC 68682-170-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V041000·2021-02-02

    Shyft Group Recalls 2020-2021 Spartan K2, K3, K4 RV Chassis

    Shyft Group is recalling 2020-2021 Spartan K2, K3, and K4 RV chassis because steering gear mounting fasteners may come loose, potentially interfering with steering components and increasing crash risk.

    Product
    SPARTAN — SPARTAN K2, K3, K4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E007000·2021-02-01

    Howmet Aerospace Recalls Alcoa High Polish Aluminum Wheels

    Howmet Aerospace is recalling specific Alcoa High Polish Aluminum Wheels that may bend or break under load, increasing the risk of a crash.

    Product
    WHEELS:RIM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V037000·2021-02-01

    2021 RAM 1500 trucks recalled for missing brake pedal retaining clip

    Chrysler is recalling certain 2020-2021 RAM 1500 trucks built without a retaining clip securing the brake pedal to the brake system. The missing clip can cause the brake pedal to separate, preventing drivers from applying the brakes and increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V039000·2021-02-01

    Micro Bird Recalls G5 Buses Due to Wiring Fire Risk

    Micro Bird is recalling 2013-2021 G5 school and transit buses because damaged electrical wiring behind the driver's seat may cause a short circuit or fire.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V038000·2021-02-01

    2021 Volkswagen Jetta front seat bolts missing, increasing crash injury risk

    Volkswagen is recalling 2021 Jetta and Tiguan vehicles because bolts may be missing from front seat tracks. Missing bolts allow seats to move freely, increasing the risk of injury in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E006000·2021-02-01

    Putco Recalls Nitro-Lux LED Headlamp Bulbs for Excessive Glare

    Putco is recalling specific Nitro-Lux LED headlamp bulbs because they may cause excessive glare to oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V036000·2021-02-01

    Micro Bird Recalls G5 Buses Due to Wiring Fire Risk

    Micro Bird is recalling 2014-2021 G5 School and Transit Buses because damaged electrical wiring behind the driver's seat could cause a short circuit and fire.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V034000·2021-01-29

    2021 Mercedes-Benz ISOFIX Bracket May Be Missing From Child Restraint Anchor

    Mercedes-Benz is recalling certain 2021 A220, A35 AMG, and CLA250 vehicles because the ISOFIX child seat anchoring bracket on the right-rear seat may be missing the right-side anchoring bar, preventing proper restraint of child car seats.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220, CLA 250, AMG A35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V031000·2021-01-29

    2021 BMW X5, X6, X7 Steering Column Defect Recall

    BMW is recalling certain 2021 X5, X6, and X7 models due to a defect in the steering column shaft universal joint that may not be tightened to specifications, potentially affecting vehicle handling and control.

    Product
    BMW — BMW X6, X5, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V035000·2021-01-29

    Tesla Recalls Model S and X for Display Memory Wear

    Tesla is recalling 2012-2018 Model S and 2016-2018 Model X vehicles because center display memory wear can cause loss of rearview camera and turn signals.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide