The Recall Desk

State

Delaware product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

301–325 of 77014

  • ModerateFDA (Devices)·Z-0021-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling 156 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8" X 2.5" 1-LINE (CS 12) LIGHT BLUE Model/Catalog Number: A70107000 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3325-2026·2026-10-07

    Percussionaire Recalls Intrapulmonary Percussive Ventilation Devices Due to Labeling Warning

    Percussionaire Corporation is recalling 419 Intrapulmonary Percussive Ventilation (IPV) devices to update labeling warnings regarding the use of volatile anesthetic delivery systems.

    Product
    Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0068-2027·2026-10-07

    Illumina NovaSeq 6000Dx Recalled for Server Security Vulnerability

    Illumina is recalling 80 NovaSeq 6000Dx and DRAGEN Server units worldwide due to a security vulnerability in the server component.

    Product
    NovaSeq 6000Dx including DRAGEN Server, Catalog Number: 20068232; Illumina DRAGEN Server for NextSeq 550Dx, Catalog Number: 20086130
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0048-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling 6,510 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 44" X 4" 2-Line, Green Model/Catalog Number: ASP-564015 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3321-2026·2026-10-07

    Percussionaire Recalls Intrapulmonary Percussive Ventilation Devices Due to Labeling Warning

    Percussionaire Corporation is recalling IPV-1C and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.

    Product
    Intrapulmonary Percussive Ventilation, IPV-1C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used with Instruction Manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0028-2027·2026-10-07

    Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates

    ASP Global is recalling Expressaire disposable tourniquet cuffs due to incorrect expiration dates. The products were labeled with a 10-year shelf life, but the validated shelf life is 5 years.

    Product
    Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 18" X 4" 2-LINE (CS 18) RED Model/Catalog Number: A70107007 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3315-2026·2026-10-07

    Philips SmartPath to MR 7700 Recalled for Incorrect DTI Export Data

    Philips is recalling five SmartPath to MR 7700 units because diffusion tensor imaging exports contain incorrect data, preventing correct processing by third-party software.

    Product
    SmartPath to MR 7700; Model number (REF): 1. 782178, 2. 782207; Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3273-2026·2026-10-07

    Alere hCG Urine Test Strips Recalled for False Positive Risk

    Alere San Diego is recalling multiple hCG urine test strips because they may detect low hCG levels, resulting in false positive results.

    Product
    Fisher Scientific Sure-Vue Urine hCG Strip, Model/ Part: FHC-101/23900527; McKesson CONSULT hCG Urine Test Dipstick CLIA Waived, Model/ Part:FHC-101/5000; Henry Schein One Step+ hCG Urine Strip Test, Model/ Part: FHC-101/9004072; Alere hCG Dipstick (25mIU/mL) in Urine, Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0009-2027·2026-10-07

    FDA Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 18" X 4" 2-LINE (CS 10) RED Model/Catalog Number: 564007 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3332-2026·2026-10-07

    Beckman Coulter AU480 Chemistry Analyzer Software Error Recall

    Beckman Coulter is recalling AU480 Chemistry Analyzers because a software error prevents the instrument from starting, delaying patient results.

    Product
    Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 / 14987666542965 B96693 / 14987666542972 B12183 / 14987666540671 The AU480 Chemistry Analyzer measure analytes in samples, in combination with appropriate…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0043-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 30" X 4" 1-Line, White Model/Catalog Number: ASP-564010 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0011-2027·2026-10-07

    FDA Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 24" X 4" 2-LINE (CS 10) YELLOW Model/Catalog Number: 564009 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0020-2027·2026-10-07

    Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates

    ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 38" X 4" 1-LINE (CS 10) Model/Catalog Number: 564044 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3288-2026·2026-10-07

    United Imaging uMI 780 PET/CT System Software Recall

    Shanghai United Imaging Healthcare is recalling one uMI 780 PET/CT system due to a software defect that may hide patient images, potentially requiring rescans.

    Product
    Positron Emission Tomography and Computed Tomography System, Model: uMI 780
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0060-2027·2026-10-07

    ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling 360 MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE (10) Model/Catalog Number: DT-7044-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2027·2026-10-07

    Ajanta Pharma Recalls Ranolazine Tablets for Dissolution Failure

    Ajanta Pharma USA Inc. is recalling Ranolazine Extended-Release Tablets, 1000 mg, because the product failed to meet dissolution specifications.

    Product
    RANOLAZINE — RANOLAZINE (RANOLAZINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0041-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

    Product
    Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-Line, Yellow Model/Catalog Number: ASP-564008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3285-2026·2026-10-07

    United Imaging uMI Panorama GS PET/CT Systems Recalled for Software Defect

    Shanghai United Imaging Healthcare is recalling three uMI Panorama GS PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.

    Product
    Positron Emission Tomography and Computed Tomography System, Model: uMI Panorama GS with software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3312-2026·2026-10-07

    Philips MR 5300 Recalled for Incorrect Diffusion Tensor Imaging Data

    Philips North America is recalling 131 MR 5300 systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.

    Product
    MR 5300; Model number (REF): 1. 782110, 2. 782152, 3. 782156, 4. 782196; Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3272-2026·2026-10-07

    Alere Recalls hCG Pregnancy Tests Due to False Positive Risk

    Alere San Diego, Inc. is recalling multiple hCG pregnancy test models because they may detect low hCG levels, resulting in false positive results.

    Product
    Fisher Scientific Sure-Vue Serum/Urine hCG, Model/ Part: FHC-202/23900529, FHC-202/23900528; Beckman Coulter Inc's ICON 25 hCG, Model/ Part: FHC-202/43025; Henry Schein One Step+ hCG Combo test in Serum or Urine, Model/ Part: FHC-202/9004075; Alere hCG Combo Cassette…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0045-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

    Product
    Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 34" X 4" 1-Line, Blue Model/Catalog Number: ASP-564012 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3314-2026·2026-10-07

    Philips Recalls SmartPath MRI Software Due to Incorrect DTI Export Data

    Philips is recalling SmartPath MRI software because it exports incorrect diffusion tensor imaging data, preventing correct processing by third-party tractography software.

    Product
    SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, and SmartPath to Ingenia Elition X; Model number (REF): 1. 781260 (1.5T), 2. 782112 (1.5T), 3. 782146 (1.5T), 4. 782165 (1.5T), 5. 782145 (3.0T), 6. 782164 (3.0T), 7. 781270 (XR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3311-2026·2026-10-07

    Philips Recalls Ingenia MRI Systems Due to Incorrect DTI Export Data

    Philips is recalling 340 Ingenia MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate third-party processing.

    Product
    Ingenia Elition S and Ingenia Elition X.; Model number (REF): 1. 781357 (S), 2. 782106 (S), 3. 782137 (S), 4. 782157 (S), 5. 781358 (X), 6. 782107 (X), 7. 782119 (X), 8. 782136 (X), 9. 782158 (X), 10. 782198 (X); Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3286-2026·2026-10-07

    United Imaging uMI Panvivo PET/CT Systems Recalled for Software Defect

    Shanghai United Imaging Healthcare is recalling three uMI Panvivo PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.

    Product
    Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo with software
    Category
    Medical Device
    Distribution
    Distributed nationwide