The Recall Desk

State

Massachusetts product recalls

72,913 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 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2026–2050 of 81121

  • ModerateFDA (Devices)·Z-2122-2026·2026-05-13

    Medline Convenience Kits sterilization calibration issue recalled

    Medline is recalling Convenience Kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2132-2026·2026-05-13

    ZENBONE Resorbable Bone Void Filler Recall Outside Specifications

    Orthorebirth Co Ltd is recalling ZENBONE resorbable bone void filler because the product falls outside standard specifications. The recall affects specific lot numbers distributed nationwide in California and Florida.

    Product
    ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-Z
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2086-2026·2026-05-13

    Uric Acid in vitro diagnostic test distributed without FDA clearance

    DFI Co., Ltd. is recalling its Uric Acid in vitro diagnostic test (REF: 31H0P) because the devices were distributed without required FDA premarket clearance or approval.

    Product
    Uric Acid in vitro diagnostic test REF: 31H0P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2099-2026·2026-05-13

    Medline Convenience Kits Recalled for Potential Sterilization Calibration Issues

    Medline Industries is recalling multiple convenience kits due to calibration issues with sterilization and packaging equipment that may compromise sterility assurance. Approximately 5,497 units were affected and distributed nationwide.

    Product
    See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) BREAST-HERNIA-PORT CDS-LF, Model Number: CDS984853J; 3) KIT UROLOGY URETHROPLASTY, Model Number: DYKMBNDL117C; 4) KIT PLASTIC INSERT TISSUE EXPA, Model Number: DYKMBNDL158
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2074-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps recalled for instruction updates

    Katalyst Surgical is issuing a Field Safety Corrective Action for 670 units of DEX Ophthalmic Tissue Forceps (Model DVF4019-25) due to updates required in the instructions for use. The device was distributed worldwide.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2073-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps 23ga Maculorhexis Forceps Recalled

    Katalyst Surgical, LLC is recalling DEX Ophthalmic Tissue Forceps, Model DVF4019-23, due to a field safety corrective action for instructions for use in DEX Forceps and Scissors. The device is distributed worldwide.

    Product
    DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0511-2026·2026-05-13

    Buspirone Hydrochloride Tablets 5 mg Recalled for Subpotency

    Unichem Pharmaceuticals USA Inc. is recalling Buspirone Hydrochloride Tablets, USP, 5 mg because the drug is subpotent. The recall affects approximately 10,875 bottles distributed nationwide.

    Product
    BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V299000·2026-05-12

    Ford Bronco hardtop roof panel sections may separate and detach

    Ford is recalling certain 2021-2022 Bronco vehicles because Molded-In-Color hardtop roof panels may have been manufactured improperly, allowing outer sections to detach.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V302000·2026-05-12

    Vespa Motorcycles Recalled for Missing Rearview Mirror Warning Label

    Piaggio Group Americas is recalling 285 specific Vespa models because the rearview mirrors lack the required convex mirror warning text.

    Product
    VESPA — VESPA GTV 310, PRIMAVERA 150, PRIMAVERA 50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E029000·2026-05-12

    Hiab Recalls Waltco MDV Series Liftgates Due to Deck Pin Failure Risk

    Hiab USA Inc. is recalling certain Waltco MDV series liftgates because deck pins may break, causing the platform to fall and increasing injury risk.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V301000·2026-05-12

    Ford Recalls 2026 Escape and Lincoln Corsair for Park Module Failure

    Ford is recalling 2026 Escape and Lincoln Corsair vehicles because the park module may fail to lock, increasing the risk of the vehicle rolling away and causing a crash.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V297000·2026-05-12

    2026 Land Rover Range Rover vehicles recalled for faulty seat belt warning

    Jaguar Land Rover is recalling certain 2026 Range Rover Velar, Range Rover Sport, and Range Rover vehicles because the seat belt warning chime may not sound when occupants are unbuckled, increasing crash injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER VELAR, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V300000·2026-05-12

    Nova Bus speaker hole doors are missing the glazing DOT mark

    Nova Bus is recalling certain LFS transit buses because the driver's speaker hole door may lack the prime glazing manufacturer DOT code mark, breaching FMVSS 205.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E028000·2026-05-11

    Beck/Arnley Replacement Lower Control Arm and Ball Joint Recall

    Federal-Mogul Motorparts is recalling Beck/Arnley replacement lower control arm and ball joint assemblies for 2018-2025 Subaru Forester and Crosstrek vehicles due to loose nuts.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V294000·2026-05-11

    International Recalls 2026-2027 HV Trucks for Brake Release Delay

    International is recalling 2026-2027 HV vehicles because the service brake may take longer than expected to release, increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V296000·2026-05-11

    2024 Chrysler Pacifica wheelchair restraints may not lock properly

    Braun Corporation is recalling certain 2023–2026 Chrysler Pacifica vehicles because wheelchair retractors may not lock, preventing proper securement. An unsecured wheelchair can move during transit and increase injury risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V295000·2026-05-11

    Forest River Recalls 2026 Prime Time Crusader Trailers for Sewer Gas Risk

    Forest River is recalling 2026 Prime Time Crusader recreational trailers because the waste water ventilation pipe may end inside the trailer, allowing sewer gas to enter the cabin.

    Product
    PRIME TIME — PRIME TIME CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V293000·2026-05-08

    Fly Wing Snake 250 EFI Motorcycles Recalled for Brake Pad Defect

    NHTSA is recalling 2024 Fly Wing Snake 250 EFI motorcycles because brake pads may fail in wet conditions, increasing crash risk.

    Product
    FLY WING — FLY WING SNAKE 250 EFI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E027000·2026-05-08

    Dometic Recalls Fan-Tastic Vent Fans Due to Missing Hinge Pin

    Dometic is recalling specific Fan-Tastic Vent Fans because a missing hinge pin allows the lid to detach, creating a road hazard for other vehicles.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V292000·2026-05-08

    Shyft Recalls Spartan RV Chassis Vehicles Due to Brake Light Defect

    Shyft Group is recalling specific Spartan RV chassis vehicles because the exterior brake lights may remain illuminated when the brakes are not applied, increasing crash risk.

    Product
    SPARTAN — SPARTAN RV CHASSIS K3, RV CHASSIS K2, RV CHASSIS K4, RV CHASSIS K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26465·2026-05-07

    EEMB Lithium Battery Packs Recalled for Unsafe Child-Resistant Packaging

    EEMB lithium coin battery packs sold online are not in child-resistant packaging as required by law. If swallowed by a child, these batteries can cause serious internal injuries or death.

    Product
    EEMB Lithium Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26468·2026-05-07

    Svnntaa Bed Rails Recalled Due to Entrapment and Asphyxiation Risk

    Svnntaa bed rails sold on Amazon violate safety standards and pose a risk of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact Eokeanon for a refund.

    Product
    Svnntaa Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V288000·2026-05-07

    RAM Recalls 2023-2026 Ram 2500 Trucks for Software Error

    Chrysler is recalling 2023-2026 Ram 2500 trucks because a software error may allow vehicle speed to exceed tire ratings, risking loss of control.

    Product
    RAM — RAM 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26475·2026-05-07

    Analemma Water Bottles recalled for laceration and ingestion hazards

    Analemma Water Bottles are recalled because the inner glass liner can break, posing risk of serious injury or death from laceration and ingestion. The importer has received 20 reports of the glass breaking, including one oral injury.

    Product
    Analemma Water Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26477·2026-05-07

    Youth Sweatshirts with Drawstrings Recalled for Strangulation Hazard

    Allura Imports is recalling about 120 youth sweatshirts with drawstrings due to risk of strangulation. The drawstrings can catch on objects and cause serious injury or death to children.

    Product
    Youth Sweatshirts with Drawstrings
    Category
    Consumer Product
    Distribution
    Distributed nationwide