The Recall Desk

State

Massachusetts product recalls

72,940 recalls have nationwide distribution and so reach Massachusetts. 8,209 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,209
Critical
1,171
Severe
2,013
Most recent
2026-09-09

Of the 8,209 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 2,013 (25%) are Severe.

These figures cover only the 8,209 recalls whose distribution notice names Massachusetts specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3651–3675 of 81149

  • HighCPSC·26203·2026-01-22

    Treadmills recalled over power cords that can loosen from the socket

    About 47,000 Matrix and Vision treadmills are being recalled because the power cord can become loose from the power socket, posing a fire hazard.

    Product
    Matrix Retail T30, TF30, T50, TF50, and T75 treadmills, Vision T9800, TF20, T40, and T80 treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26202·2026-01-22

    Folding rocker chairs recalled over legs that can break

    About 35,300 Magellan Odyssey Rocker Chairs sold by Academy Sports + Outdoors are being recalled because the chairs' legs can break.

    Product
    Magellan Odyssey Rocker Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26208·2026-01-22

    Magnetic stick figure toy sets recalled over loose ingestible magnets

    About 1,600 Vndueey Magnetic Men toy sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.

    Product
    Vndueey Magnetic Men Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26206·2026-01-22

    Torch lighters recalled over a lack of child-resistant mechanisms

    About 7,500 Topkay Torch Lighters are being recalled because they do not have the child-resistant mechanisms required by the mandatory standard for multipurpose lighters.

    Product
    Topkay Torch Lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V032000·2026-01-22

    Blue Bird Recalls 2026-2027 School Buses for Illegible Window Markings

    Blue Bird is recalling 2026-2027 Vision and All American school buses because side and rear windows may have illegible DOT markings, failing federal safety standards.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V033000·2026-01-22

    Blue Bird Recalls One 2026 Vision Transit Bus for Window Markings

    Blue Bird is recalling one 2026 Vision transit bus because side or rear windows may have illegible DOT markings, failing federal safety standards.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1021-2026·2026-01-21

    Libre 3 Plus sensors recalled in a second lot over carbon build up

    Abbott Diabetes Care is recalling 1,663,241 FreeStyle Libre 3 Plus sensors, REF 78768-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Food)·H-0405-2026·2026-01-21

    Hingwastika churna supplement recalled over potential undeclared wheat

    Herbs Forever is recalling 45 units of HerbsForever Hingwastika Churna Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The action is Class I.

    Product
    HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0399-2026·2026-01-21

    Plant-based almondmilk chocolate bars recalled over undeclared hazelnut

    Fran's Chocolates is recalling 112 units of Fran's PureBar Almondmilk Chocolate 46% Madagascar over undeclared hazelnut. The FDA has classified the action as Class I.

    Product
    Fran s PureBar Almondmilk Chocolate 46% Madagascar Plant-Based, net wt. 1.1oz, UPC 7 49668 24280 2. Ingredients: Sugar, cocoa butter, cocoa beans, almonds, sunflower lecithin, vanilla extract. May contain traces of milk, peanuts and sesame. Fran's Chocolates, Ltd. Seattle, WA
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1052-2026·2026-01-21

    Holiday cookie tins recalled over undeclared almond, pecan and walnut

    One Roof LLC is recalling 197 Atwater's Holiday Cookie Tins over undeclared tree nut allergens: almonds, pecans and walnuts.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1020-2026·2026-01-21

    Glucose monitoring sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1023-2026·2026-01-21

    Libre 3 Plus sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1022-2026·2026-01-21

    Libre 3 Plus sensors, REF 78769-01, recalled over carbon build up

    Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Food)·H-0404-2026·2026-01-21

    Ayurvedic gastro supplement recalled over potential undeclared wheat

    Herbs Forever is recalling 45 units of HerbsForever Gastro Care Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The FDA has classified the action as Class I.

    Product
    HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V024000·2026-01-21

    Ford Recalls 2026 Explorers for Windshield Bonding Defect

    Ford is recalling 2026 Explorer vehicles because the windshield may not be properly bonded, posing an injury risk in a crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0269-2026·2026-01-21

    Excedrin recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Excedrin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    EXCEDRIN 2'S DISP.- 30 CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1058-2026·2026-01-21

    Children's NyQuil recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Children's NyQuil Cold & Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) ADMIN KIT, Medline kit SKU DYKS1339B; 2) ADMIN KIT, Medline kit SKU DYKS1339C; 3) QCASC WELCOME KIT, Medline kit SKU DYKS1359B; 4) ADMISSION KIT, Medline kit SKU DYKS
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0261-2026·2026-01-21

    Frozen raw shrimp recalled over elevated levels of chloramphenicol

    AZ Gems is recalling 1,099 cases of Member's Mark Jumbo Raw Shrimp over elevated levels of chloramphenicol.

    Product
    Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559
    Category
    Food
    Distribution
    Distributed nationwide