The Recall Desk

State

Massachusetts product recalls

72,971 recalls have nationwide distribution and so reach Massachusetts. 8,211 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,211
Critical
1,171
Severe
2,013
Most recent
2026-09-16

Of the 8,211 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 8,211 recalls whose distribution notice names Massachusetts specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6426–6450 of 81182

  • ModerateFDA (Devices)·Z-2011-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screw package labeling mismatch

    Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because the package labeling lists a different size than the actual product included inside.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm Model/Catalog Number: 506-04-130 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-1998-2025·2025-07-02

    LUCAS Chest Compression System demonstration units recalled

    Jolife AB is recalling LUCAS 2, 3, and 3.1 chest compression system demonstration units that may have been provided to customers for clinical use instead of demonstration purposes only.

    Product
    LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1995-2025·2025-07-02

    Medline Umbilical Tray sterile packaging defect recall

    Medline is recalling umbilical trays due to a possible packaging defect in the outer Tyvec pouch that protects the sterile product. The defect may compromise sterility.

    Product
    Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0092-2025·2025-07-02

    Super ProTHIN Plus Dietary Supplement Recalled for Undeclared Dyes

    Preventics, Inc. dba Legere Pharmaceuticals is recalling Super ProTHIN Plus dietary supplement because gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food colorings.

    Product
    Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2025·2025-07-02

    Caphosol Artificial Saliva sachets recalled for out-of-specification stability

    Recordati Rare Diseases is recalling Caphosol Artificial Saliva 32-dose sachets because stability test results for Solution B were out of specification during process validation.

    Product
    Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 mL sachets aqueous solution (32 sachets Solution A Phosphate, 32 sachets Solution B Calcium)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2009-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screw labeling mismatch recall

    Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling lists a different size than the actual product included inside.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm Model/Catalog Number: 506-04-122 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-2026-2025·2025-07-02

    Jewel Precision Reusable Rigid Sterilization Container System Instructions Mismatch

    Jewel Precision Reusable Rigid Sterilization Container System (Model JP-24-6) is being recalled because the Instructions for Use do not match the FDA-cleared indications for use or sterility shelf life.

    Product
    Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog Number: JP-24-6.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0483-2025·2025-07-02

    Tirzepatide Injections Pre-filled Syringe Recalled for Sterility Assurance

    Thrive Health Solutions is recalling Tirzepatide Injections 20mg/mL pre-filled syringes due to lack of assurance of sterility. Approximately 826 syringes distributed nationwide are affected.

    Product
    Tirzepatide Injections, 20mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0093-2025·2025-07-02

    Protrim Plus Dietary Supplement Recall for Undeclared Food Dyes

    Protrim Plus dietary supplement 90-capsule bottles contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules. The product was distributed nationwide and may pose a risk to consumers with dye sensitivities or allergies.

    Product
    Protrim Plus, dietary supplement. 90 capsule/bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0095-2025·2025-07-02

    NutriLean Dietary Supplement Contains Undeclared Food Dyes

    Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplements nationwide because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes, which are not listed on the label.

    Product
    NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0096-2025·2025-07-02

    Rodex Forte dietary supplement recalled for undeclared food dyes

    Rodex Forte dietary supplement (90-capsule bottles) is being recalled because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1), which are not listed on the label.

    Product
    Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V434000·2025-06-30

    Volkswagen chassis, brake and suspension bolts may be incorrectly tightened

    Volkswagen is recalling certain 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 vehicles because bolts on the chassis, brake system and suspension may not have been correctly tightened in manufacturing.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS, ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V428000·2025-06-27

    Audi Recalls 2025 E-Tron GT Vehicles Due to Suspension Strut Defect

    Volkswagen Group of America is recalling 2025 Audi E-Tron GT vehicles because a retaining ring on the front suspension strut may come loose, potentially causing air loss and loss of vehicle control.

    Product
    AUDI — AUDI E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V443000·2025-06-27

    Ford Recalls 2017 GT Models for Rear Wing Hydraulic Leak Risk

    Ford is recalling 2017 GT vehicles previously repaired under recall 18V707 because the rear wing valve block may leak hydraulic fluid, increasing fire risk.

    Product
    FORD — FORD GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V440000·2025-06-27

    Freightliner Recalls 2026 Cascadia Fifth Gen Trucks for Fuel Line Routing Defect

    Daimler Trucks North America is recalling 2026 Freightliner Cascadia Fifth Gen trucks because an incorrectly routed fuel line can damage brake lines and wiring, increasing crash and fire risks.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA FIFTH GEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V439000·2025-06-27

    Ford Expedition and Navigator passenger airbags may deploy with excessive force

    Ford is recalling certain 2025 Navigator and Expedition vehicles because the passenger side airbag may have been manufactured incorrectly and can deploy with excessive force during a crash.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V445000·2025-06-27

    Orange EV Recalls HUSK-E Trucks for Electrical Fire Risk

    Orange EV is recalling 2023-2025 HUSK-E terminal trucks because an incorrect washer size installed during a previous repair can cause electrical arcing and increase the risk of fire.

    Product
    ORANGE EV — ORANGE EV HUSK-E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V441000·2025-06-27

    Ford Recalls 2022 Mustang Mach E Vehicles for Battery Contactor Overheating

    Ford is recalling 2022 Mustang Mach E vehicles with extended range batteries because high voltage contactors may overheat, potentially causing loss of drive power and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V437000·2025-06-27

    Nissan and Infiniti VC-Turbo engine bearings may cause engine failure

    Nissan is recalling certain 2019-2024 Rogue, Altima, Infiniti QX50 and QX55 vehicles with VC-Turbo engines because engine bearing defects can lead to engine failure and, if the block is breached, an engine fire.

    Product
    INFINITI — INFINITI, NISSAN QX55, ALTIMA, QX50, ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V431000·2025-06-27

    Newmar motorhome baggage door skins can separate from the door frame

    Newmar is recalling certain 2016-2024 King Aire, 2023-2024 London Aire and Essex motorhomes because the baggage door skins may come loose and separate from the door frame.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V438000·2025-06-27

    Ford Recalls 2025 F-150 Lightning BEV Due to Brake Hose Bracket Issue

    Ford is recalling 2025 F-150 Lightning BEV vehicles because front brake jounce hose bracket screws may loosen, causing a brake fluid leak that increases stopping distance.

    Product
    FORD — FORD F-150 LIGHTNING BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V444000·2025-06-27

    Oshkosh Recalls 2025 NGDV Vehicles for Detaching Air Bag Warning Label

    Oshkosh is recalling 2025 NGDV and NGDV Electric vehicles because the air bag warning label on the sun visor may detach, failing federal safety standards.

    Product
    OSHKOSH — OSHKOSH NGDV ELECTRIC, NGDV
    Category
    Vehicle
    Distribution
    Distributed nationwide