The Recall Desk

State

Massachusetts product recalls

73,198 recalls have nationwide distribution and so reach Massachusetts. 8,240 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,240
Critical
1,181
Severe
2,025
Most recent
2026-09-30

Of the 8,240 recalls naming Massachusetts we have scored against our rubric, 1,181 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,025 (25%) are Severe.

These figures cover only the 8,240 recalls whose distribution notice names Massachusetts specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14251–14275 of 81438

  • SevereFDA (Food)·F-0551-2024·2023-12-20

    Wilcox Premium Pumpkin ice cream recalled due to Listeria contamination

    Wilcox Premium Pumpkin ice cream in multiple sizes is being recalled due to potential Listeria monocytogenes contamination. Affected products distributed in VT, NH, MA, and NY with Best By dates from September to November 2024.

    Product
    Wilcox Premium Pumpkin in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0559-2024·2023-12-20

    Wilcox Premium Cream and Coffee Fudge recalled for Listeria contamination

    Wilcox Premium Cream and Coffee Fudge ice cream in multiple sizes is being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with Best By dates from September through November 2024.

    Product
    Wilcox Premium Cream and Coffee Fudge in 1.5QT, Quart, and Pint sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0593-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in gift baskets due to undeclared tree nuts allergen. Consumers with tree nut allergies should not consume these products.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #359 Brownie, Cookie & Cake Sleigh
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0564-2024·2023-12-20

    Wilcox Premium Chocolate Raspberry Truffle ice cream recalled for Listeria contamination

    Wilcox Premium Chocolate Raspberry Truffle ice cream is recalled for potential Listeria monocytogenes contamination. Products distributed in VT, NH, MA, and NY with Best By dates 9/14/24–11/14/24 are affected.

    Product
    Wilcox Premium Chocolate Raspberry Truffle in 1.5QT, Quart, and Pint sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0547-2024·2023-12-20

    Wilcox Premium Raspberry Cheesecake Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Raspberry Cheesecake ice cream may be contaminated with Listeria monocytogenes. The recall affects products distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates from 9/14/24 to 11/14/24.

    Product
    Wilcox Premium Raspberry Cheesecake in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0532-2024·2023-12-20

    Leonardo's Gelato Chocolate Gelato Recalled for Listeria Contamination

    Wilcox Ice Cream is recalling Leonardo's Gelato Chocolate Gelato due to potential Listeria monocytogenes contamination. The recall affects pints and 4 oz cups distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Leonardo's Gelato Chocolate Gelato; Pints (UPC 8 1643900005) and 4 oz cup (UPC 81643900028)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0548-2024·2023-12-20

    CereLink ICP Extension Cable Recalled for Out of Range Readings

    Integra LifeSciences is recalling CereLink ICP Extension Cables due to a design defect causing out of range readings. The Class I recall affects 4,941 units distributed nationwide and internationally.

    Product
    CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP) Monitor, Model No. 826820/826820P. Cable is also provided with monitor as part of the same SKU.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0557-2024·2023-12-20

    Wilcox Premium Maple Cheesecake ice cream recalled for potential Listeria contamination

    Wilcox Ice Cream is recalling Wilcox Premium Maple Cheesecake due to potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Premium Maple Cheesecake in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0594-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling 4,875 Acorn Raspberry Creme Filled Cookies from gift baskets due to undeclared tree nut allergen. These products were distributed across all U.S. states.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #373 Cookie, Brownie and Cake Winter Assortment
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0538-2024·2023-12-20

    Wilcox Premium Maple Walnut Ice Cream Products Recalled Due to Listeria

    Wilcox Premium Maple Walnut ice cream in multiple sizes has been recalled due to potential Listeria monocytogenes contamination. Products were distributed in VT, NH, MA, and NY with best-by dates from September to November 2024.

    Product
    Wilcox Premium Maple Walnut in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0520-2024·2023-12-20

    Wilcox Vanilla Ice Cream Recalled for Possible Listeria Contamination

    Wilcox SUPER PREMIUM Vanilla ice cream (1.5 QT and Pint sizes) may be contaminated with Listeria monocytogenes. Products were distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates September 13 to November 14, 2024.

    Product
    Wilcox SUPER PREMIUM Vanilla; 1.5 QT (UPC 04372601519) and Pint (UPC 04372601619)
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0543-2024·2023-12-20

    Medical Diagnostic System Recall Due to Software-Related System Freezes and Delayed Results

    Ortho-Clinical Diagnostics is recalling the VITROS 3600 Immunodiagnostic System due to software issues causing system freezes and delayed test result reporting. The delays could affect patient care when rapid results are critical.

    Product
    VITROS 3600 Immunodiagnostic System Product Code 6802783 and Refurbished Product Code 6802914 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2024·2023-12-20

    Medical Device Recall: Para-Pak Zn-PVA Stool Collection Vials for Leakage Risk

    Meridian Bioscience is recalling Para-Pak Zn-PVA stool specimen collection vials due to a manufacturing defect that may cause leakage and risk exposure to biological hazards.

    Product
    Para-Pak Zn-PVA/10% Formalin-for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites Catalog Number: 301012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0528-2024·2023-12-20

    Sterile PVP Medical Solution Recalled for Non-Sterile Contents

    Medline Industries is recalling 700 units of Sterile PVP solution because the labeling claims sterility but the contents are non-sterile. The affected products were distributed nationwide in eight states.

    Product
    STERILE PVP, REF DYNDA1649
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0519-2024·2023-12-20

    Para-Pak Clean Vial Stool Collection Kits Recalled for Manufacturing Defect

    Meridian Bioscience is recalling Para-Pak Clean Vials used for stool specimen collection due to a manufacturing defect that increases leakage risk and may expose users to biological hazards.

    Product
    Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V864000·2023-12-20

    2022-2023 Toyota Corolla Cross air bag deployment defect recall

    Toyota is recalling 2022-2023 Corolla Cross vehicles where instrument panel defects may prevent the front-passenger air bag from deploying in a crash. Dealers will replace the panel at no cost.

    Product
    TOYOTA — TOYOTA COROLLA CROSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0510-2024·2023-12-20

    Wilcox Premium Coffee Recalled Due to Listeria Contamination

    Wilcox Premium Coffee products with Best By dates from September 14 to November 14, 2024, may be contaminated with Listeria monocytogenes. Products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Premium Coffee; 4 oz Cup; UPC 04372600403; Wilcox Premium Coffee in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0527-2024·2023-12-20

    Sterile Prep Stick Recall: Non-Sterile Contents Despite Sterile Labeling

    Medline Industries is recalling sterile prep sticks (REF DYNDA1134) labeled as sterile that contain non-sterile solution, posing infection risk in medical procedures.

    Product
    STERILE STERILE PREP STICK, REF DYNDA1134
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V865000·2023-12-20

    Toyota and Lexus vehicles recalled for air bag sensor short circuit defect

    Toyota and Lexus are recalling certain 2020-2022 vehicles with a faulty Occupant Classification System sensor that may prevent the front passenger air bag from deploying in a crash, increasing injury risk.

    Product
    LEXUS — LEXUS, TOYOTA ES, CAMRY HYBRID, AVALON, ES HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0523-2024·2023-12-20

    Collision Sensor Malfunction in Siemens ARTIS Icono Fluoroscopic X-Ray System

    The ARTIS icono fluoroscopic x-ray system may falsely detect collisions for up to 30 minutes after startup, requiring manual override with reduced safety protection and limiting diagnostic use.

    Product
    ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0551-2024·2023-12-20

    Medical imaging software incorrectly displays patient studies to wrong patients

    Change Healthcare's Stratus Imaging PACS software can incorrectly associate patient imaging studies with the wrong patients. Approximately 454 affected units have been distributed nationwide.

    Product
    Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4, a component of Stratus Imaging PACS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2024·2023-12-20

    Povidone Solution Labeled Sterile Despite Non-Sterile Contents

    Medline Industries recalls 300 units of Sterile Povidone (REF DYNDA2061) after discovering the solution inside foil sachets is non-sterile despite sterile labeling. Affected lots are distributed across eight states.

    Product
    STERILE POVIDONE, REF DYNDA2061
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V867000·2023-12-20

    Audi E-Tron Battery Modules May Overheat Creating Fire Risk

    Audi is recalling 2019-2022 E-Tron vehicles because high-voltage battery modules may overheat and increase fire risk. Dealers will install diagnostic software and replace affected modules at no cost.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0529-2024·2023-12-20

    Medline PVP Solution Recalled Due to Mislabeled Sterility

    Medline PVP Solution (REF DYNDA1858) is being recalled because it is labeled as sterile but contains non-sterile contents. 1,950 units are affected.

    Product
    PVP SOLUTION SING STRL, REF DYNDA1858
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0553-2024·2023-12-20

    X-ray system overhead suspension components may fall due to incorrect bolt torque

    GE HealthCare Definium Tempo and Tempo Pro X-ray systems may have been assembled with incorrect bolt torque, creating a risk that Overhead Tube Suspension components could fall.

    Product
    The System is designed as a modular system with components that include an Overhead Tube Suspension with tube/collimator, wallstand, Table, X-ray generator, and cleared wireless digital detectors. The list of detectors verified and validated for use with the Discovery XR656 HD…
    Category
    Medical Device
    Distribution
    Distributed nationwide