The Recall Desk

State

Massachusetts product recalls

73,741 recalls have nationwide distribution and so reach Massachusetts. 8,248 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,248
Critical
1,179
Severe
2,356
Most recent
2026-10-28

Of the 8,248 recalls naming Massachusetts we have scored against our rubric, 1,179 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,356 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,248 recalls whose distribution notice names Massachusetts specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34126–34150 of 81989

  • SevereFDA (Food)·F-0404-2020·2019-12-25

    Grilled Chicken & Kale Brussels Meal recalled due to possible Listeria monocytogenes contamination

    Whole Foods Market is recalling its Grilled Chicken & Kale Brussels Meal because possible contamination with Listeria monocytogenes was found. The nationwide recall covers products distributed from October 10, 2019 through November 4, 2019.

    Product
    Grilled Chicken & Kale Brussels Meal UPC 26753800000 sold in the chef's case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0396-2020·2019-12-25

    Whole Foods Recalls Chicken General Tso Due to Listeria Risk

    Whole Foods Market is recalling Chicken General Tso and Chick'n General Tso sold on the hot bar due to possible contamination with Listeria monocytogenes.

    Product
    Chicken General Tso and Chick'n General Tso sold on the hot bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0380-2020·2019-12-25

    Whole Foods Recalls Salad Broccoli Crunch Due to Listeria Risk

    Whole Foods Market is recalling Salad Broccoli Crunch due to possible Listeria monocytogenes contamination. The product was sold nationwide from October 10 to November 4, 2019.

    Product
    SALAD BROCCOLI CRUNCH served on the hot bar, salad bar, and chef's case UPC 24531600000 and UPC 24532000000
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0372-2020·2019-12-25

    Whole Foods Recalls Hot Bar Potatoes and Broccoli for Listeria Risk

    Whole Foods Market is recalling scalloped potatoes and broccoli served on the hot bar due to possible Listeria monocytogenes contamination.

    Product
    POTATOES SCALLOPED BROCCOLI & ROMESCO served on the hot bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0716-2020·2019-12-25

    Arrow Berman Angiographic Catheter Recalled for Potential Balloon Leak

    Arrow International Inc is recalling specific Arrow Berman Angiographic Catheters due to a potential leak in the balloon extension line that could cause serious injury or death.

    Product
    Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0407-2020·2019-12-25

    Whole Foods Recalls Chicken Cashew for Possible Listeria Contamination

    Whole Foods Market is recalling Chicken Cashew sold on the hot bar and in the chef's case due to possible contamination with Listeria monocytogenes.

    Product
    Chicken Cashew sold on the hot bar and in chef's case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0369-2020·2019-12-25

    Whole Foods Recalls Kale and Brussels Sprouts Salads for Listeria Risk

    Whole Foods Market is recalling various kale and Brussels sprouts salad products due to possible contamination with Listeria monocytogenes.

    Product
    Catering, Kale and Brussels Sprouts Salad Small UPC 106487 and Catering, Kale and Brussels Sprouts Salad Medium UPC 160488 served in the catering menu; Taproom, Side Kale & Brussels available in the chef's case UPC 404511; Salad, Kale & Brussels 2 For 6 UPC 22215600000 available…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0353-2020·2019-12-25

    Whole Foods Recalls Wedge Charred Corn Salad Due to Listeria Risk

    Whole Foods Market is recalling Wedge Charred Corn Salad served on the salad bar due to possible contamination with Listeria monocytogenes.

    Product
    Wedge Charred Corn Salad served on the salad bar
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0679-2020·2019-12-25

    Roche Homocysteine Test Recalled for Calibration Failures and Quality Control Issues

    Roche Diagnostics is recalling 82 units of Homocysteine tests due to calibration failures and quality control recovery issues on cobas c 701 and 702 modules.

    Product
    Roche Homocysteine-In vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c systems Catalog Number: 06542921190 - - Product Usage: The assay can assist in the diagnosis of patients suspected of having…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0384-2020·2019-12-25

    Whole Foods Recalls Salmon Dinner with Thai Curry for Listeria Risk

    Whole Foods Market is recalling Salmon Dinner with Thai Curry for 2 due to possible contamination with Listeria monocytogenes.

    Product
    Salmon Dinner with Thai Curry for 2 Packaged in the store UPC 20451500000
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0351-2020·2019-12-25

    Whole Foods Recalls Salad Bar Item for Listeria Risk

    Whole Foods Market is recalling Trend Alert Caulilini with Vadouvan Curry from salad bars due to possible Listeria monocytogenes contamination.

    Product
    Trend Alert Caulilini with Vadouvan Curry served on the salad bar
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0712-2020·2019-12-25

    Angiodynamics Recalls 60 Micro-PSD HDR Radiation Therapy Sensors

    Angiodynamics, Inc. is recalling 60 Micro-PSD HDR sensors because they may provide readings outside the expected accuracy range.

    Product
    MICRO-PSD HDR, Catalog Number: PSD-HB5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose received…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0710-2020·2019-12-25

    Angiodynamics Recalls OARtrac PLUS Clinical Detector Units Due to Accuracy Issues

    Angiodynamics, Inc. is recalling four OARtrac PLUS Clinical Detector Units because they may produce readings outside the expected accuracy range.

    Product
    OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0707-2020·2019-12-25

    Medtronic Percutaneous Pin Adapter Recall for Potential Rotation

    Medtronic is recalling 1,297 percutaneous pin adapters because they may rotate after surgical placement and fail to return to their original position.

    Product
    Medtronic Adapter Percutaneous Pin, REF 9734752 (GTIN 00643169529489) and REF 9734752-G02 (GTIN 00763000054915), contained in the following kits: Upgrade Set Percutaneous Pin, REF 9735502 (GTIN 00643169529533) and REF 9735502-G02 (GTIN 00763000208462); Medtronic Adapter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0680-2020·2019-12-25

    VisuMax Software Recall for Incorrect Corneal Cut Type During Suction Loss

    Carl Zeiss Meditec is recalling VisuMax software version 2.10.13 because a defect may cause a cap cut instead of a flap cut if suction is lost during treatment.

    Product
    VisuMax Software Version 2.10.13 with activated Software-Module ReLEx (SMILE) option used in conjunction with the VisuMax Femtosecond Laser System for Refractive Correction. Catalog Number 0000000-1345-518 Product Usage: The VisuMax Femtosecond Laser is a precision…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0338-2020·2019-12-25

    Truly Good Foods South of the Border Nut Mix Recalled for Allergen Mislabeling

    Tropical Nut & Fruit Company is recalling 106 boxes of Truly Good Foods South of the Border nut mix because the label failed to declare soy and tree nuts (almonds).

    Product
    Truly Good Foods SOUTH OF THE BORDER nut mix NET CT/WT: 25lb box, CONTAINS: PEANUTS, MILK, AND WHEAT. Distributed by Truly Good Foods, Charlotte, N.C. 28273 UPC 0 94184 11019 8
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-0386-2020·2019-12-25

    Whole Foods Recalls Grilled Caulilini for Possible Listeria Contamination

    Whole Foods Market is recalling Grilled Caulilini with Sweet Poppy Seed Sauce due to possible contamination with Listeria monocytogenes.

    Product
    Caulilini, Grilled with Sweet Poppy Seed Sauce sold in the chef's case and hot bar UPC 27268400000
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0689-2020·2019-12-25

    Teleflex Recalls Arrow EZ-IO Intraosseous Vascular Access System Needles

    Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, risking needle stick injuries and sterility compromise.

    Product
    Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit, Product Code 9001P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0706-2020·2019-12-25

    DeRoyal Warrior Recovery Knee Brace Recalled for Hinge Breakage Risk

    DeRoyal Industries is recalling Warrior Recovery Knee Braces because the hinge may break, causing the brace to come apart.

    Product
    DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0688-2020·2019-12-25

    Teleflex Recalls Arrow EZ-IO Intraosseous Vascular Access System Needles

    Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, exposing needles and compromising sterility.

    Product
    Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit, Product Code 9018P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0401-2020·2019-12-25

    Whole Foods Recalls Chicken Orange and Vegetable Meals for Listeria Risk

    Whole Foods Market is recalling Family Meal Chicken Orange and Vegetable products due to possible contamination with Listeria monocytogenes.

    Product
    Family Meal Chicken Orange and Vegetable UPC 22849900000 sold packaged in stores, PLU 28499
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0383-2020·2019-12-25

    Whole Foods Recalls Salmon Dinner with Mild Italian for Listeria Risk

    Whole Foods Market is recalling Salmon Dinner with Mild Italian for 2 due to possible contamination with Listeria monocytogenes.

    Product
    Salmon Dinner with Mild Italian for 2 packaged in the store UPC 20451300000
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0354-2020·2019-12-25

    Whole Foods Recalls Wedge Greek Salad for Listeria Risk

    Whole Foods Market is recalling Wedge Greek Salad served on the salad bar due to possible contamination with Listeria monocytogenes.

    Product
    Wedge Greek Salad served on the salad bar
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0653-2020·2019-12-25

    AuroMedics Recalls Gabapentin Capsules Due to Foreign Tablet Presence

    AuroMedics Pharma LLC is recalling specific lots of Gabapentin Capsules because a Losartan/HCTZ tablet was found in the bottles.

    Product
    Gabapentin Capsules, USP 100 mg, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 65682-198-99
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0382-2020·2019-12-25

    Whole Foods Recalls Salmon Dinner with Lemon Herb for Listeria Risk

    Whole Foods Market is recalling Salmon Dinner with Lemon Herb for 2 due to possible contamination with Listeria monocytogenes.

    Product
    Salmon Dinner with Lemon Herb for 2 packaged in the store UPC 20451100000
    Category
    Food
    Distribution
    Distributed nationwide