The Recall Desk

State

Massachusetts product recalls

72,919 recalls have nationwide distribution and so reach Massachusetts. 8,208 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,208
Critical
1,171
Severe
2,012
Most recent
2026-09-09

Of the 8,208 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,012 (25%) are Severe.

These figures cover only the 8,208 recalls whose distribution notice names Massachusetts specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2601–2625 of 81127

  • HighFDA (Devices)·Z-1760-2026·2026-04-08

    Burlington Medical caps may lose radiation attenuation over time

    Burlington Medical is recalling protective caps made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Caps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1709-2026·2026-04-08

    Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments

    Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.

    Product
    Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1686-2026·2026-04-08

    Artoura breast tissue expander infusion set needles may be blunt

    Mentor Texas is recalling Artoura Breast Tissue Expanders because the infusion sets may contain a dull or blunt needle tip that may be difficult to advance or may break.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1757-2026·2026-04-08

    Burlington Medical wrap aprons may lose radiation attenuation over time

    Burlington Medical is recalling wrap aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Wrap Aprons.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1703-2026·2026-04-08

    VOLT bone taps swapped between lots carry the incorrect thread

    The 2.4 VOLT Tap Cortex Screw is being recalled after a full lot swap with the VOLT Locking Screw Tap left the bone taps with an incorrect thread.

    Product
    2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2026·2026-04-08

    CPX 4 low height tissue expander infusion needles may be blunt

    Mentor is recalling the CPX 4 US Breast Tissue Expander with Suture Tabs, smooth low height 650 cc, because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH Smooth Low Height Tissue Expander, 650cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1739-2026·2026-04-08

    MiniMed 670G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 670G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1657-2026·2026-04-08

    Atellica hemoglobin A1c assay may return depressed patient results

    Siemens is recalling Atellica CH Enzymatic Hemoglobin A1c because results may be depressed when the RCRP reagent is processed on the same analyzer, with bias increasing over time.

    Product
    Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1665-2026·2026-04-08

    Philips Allura Xper FD20 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1699-2026·2026-04-08

    da Vinci grasping retractor instruments recalled over broken grip cables

    Intuitive Surgical is recalling da Vinci S and Si Grasping Retractor Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1748-2026·2026-04-08

    Paradigm insulin pump delivery varies with pump height changes

    Medtronic is recalling Paradigm insulin pumps models MMT-712 and MMT-715 because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    Paradigm Insulin Pump (MMT-712, MMT-715)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1746-2026·2026-04-08

    MiniMed 740G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 740G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0641-2026·2026-04-08

    Roasted peanuts recalled for undeclared banned sweetener cyclamate

    Mei Heong Yuen tangerine flavor roasted peanuts are recalled because they contain cyclamate, a sweetener banned in the U.S.

    Product
    MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super Wor
    Category
    Food
    Distribution
    19 states
  • ModerateNHTSA·26V221000·2026-04-08

    Forest River Recalls 2026 Travel Trailers Due to Incorrect Weight Labeling

    Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER AVENGER, WESTBROOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0643-2026·2026-04-08

    Mei Heong Yuen Garlic Flavor Roasted Peanuts Recalled for Banned Sweetener

    Mei Heong Yuen Garlic Flavor Roasted Peanuts (9.17 oz) are being recalled because they contain cyclamates, a banned sweetener. The product was distributed across multiple states.

    Product
    MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; U
    Category
    Food
    Distribution
    19 states
  • LowFDA (Food)·H-0642-2026·2026-04-08

    Mei Heong Yuen Walnut Flavor Roasted Peanuts recalled for banned sweetener

    Super World Trading Inc. is recalling Mei Heong Yuen Walnut Flavor Roasted Peanuts (9.17 oz) because the product contains cyclamates, a sweetener banned in the United States.

    Product
    MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Liquorice, Sugar, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trad
    Category
    Food
    Distribution
    19 states
  • LowFDA (Food)·H-0633-2026·2026-04-08

    Popping Boba RTD Peach Oolong Tea recalled for packaging integrity

    Pocas International Corp. is recalling Popping Boba RTD Peach Oolong Tea due to a packaging integrity issue that may compromise product quality.

    Product
    POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ
    Category
    Food
    Distribution
    8 states
  • LowFDA (Food)·H-0634-2026·2026-04-08

    Popping Boba RTD Mixed Berry Hibiscus Tea Packaging Integrity Recall

    Pocas International Corp. is recalling Popping Boba RTD Mixed Berry Hibiscus Tea due to a packaging integrity issue that may compromise product quality.

    Product
    POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ
    Category
    Food
    Distribution
    8 states
  • LowFDA (Food)·H-0636-2026·2026-04-08

    Popping Boba Ready-to-Drink Mango Passion Fruit Green Tea Recall

    Pocas International Corp. is recalling Popping Boba RTD Mango Passion Fruit Green Tea due to a packaging integrity issue that may compromise product quality.

    Product
    POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA 12 X 13.8OZ
    Category
    Food
    Distribution
    8 states
  • HighNHTSA·26V218000·2026-04-06

    2024 Genesis G90 seat belt anchors may detach in crash

    Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI, GENESIS SANTA FE HYBRID, IONIQ 6, SANTA FE, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V219000·2026-04-06

    Greenpower Recalls School Buses Due to Missing Mirror Warning Label

    Greenpower is recalling 2020-2024 Nano Beast and 2021-2024 Beast school buses because a warning label on the cross-view mirror may be missing, potentially increasing crash risk.

    Product
    GREENPOWER — GREENPOWER NANO BEAST SCHOOL BUS, BEAST SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V217000·2026-04-06

    Pierce Recalls Firetrucks Due to Faulty Stabilizer Indicator Light

    Pierce Manufacturing is recalling 2015-2026 aerial firetrucks because a faulty light may falsely indicate the vehicle is stable, increasing injury risk during operation.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, ARROW XT, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·PHA-04012026-01·2026-04-06

    USDA Retracts Lead Alert for Dorada Chicken Nuggets

    USDA FSIS retracted a public health alert for Dorada chicken nuggets after follow-up testing confirmed the initial lead result was a laboratory error.

    Product
    Dorada Foods — FSIS Retracts Public Health Alert for Frozen, Ready-to-Eat Chicken Nuggets Due to Updated Laboratory Result
    Category
    Food
    Distribution
    Distributed nationwide