State

Massachusetts product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32101–32125 of 81986

ModerateFDA (Devices)·Z-2068-2020·2020-05-27
Merit Medical Recalls DFINE Vertebral Assemblies Due to Incorrect Expiration Dates
Merit Medical Systems is recalling 63 DFINE Vertebral Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 3427 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1271-2020·2020-05-27
Mylan Recalls Aloprim Injection Vials Due to Discoloration
Mylan Institutional LLC is recalling 3,010 vials of Aloprim (allopurinol sodium) for Injection due to out-of-specification appearance and color results.
Product
ALOPRIM — ALOPRIM (ALLOPURINOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2089-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Hemispherical Shells because the device may fall off its post within the inner packaging, resulting in loose components and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 58 Right, Sterile, Catalog # 504-02-58D-R, UDI (01)07613327012446(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2085-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled for Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shell devices because they may fall off their post within the inner packaging, resulting in loose devices and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Right, Sterile, Catalog # 504-02-54C-R, UDI (01)07613327012415(17)
Category
Medical Device
Distribution
30 states
LowFDA (Drugs)·D-1272-2020·2020-05-27
InvaGen Recalls Gabapentin Tablets Due to Impurity Test Failure
InvaGen Pharmaceuticals is recalling 2,202 bottles of Gabapentin 600 mg tablets because they failed an impurity test during stability testing.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2038-2020·2020-05-27
Pega Medical Recalls SLIM System Handle Due to Lot Number Mismatch
Pega Medical Inc. is recalling three units of the SLIM System handle because the lot number on the instrument does not match the packaging label.
Product
Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V301000·2020-05-26
Altec Recalls Aerial Devices With Incorrect Tow Hitch Load Ratings
Altec is recalling 2014-2020 Aerial Devices with Class 3 towing hitches that may have incorrect load ratings or damage from overloading, increasing crash risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V302000·2020-05-26
2020-2021 Keystone Cougar travel trailer cooktop fire hazard
Keystone is recalling 2020-2021 Cougar travel trailers because the cooktop may not be properly sealed from the furnace, causing burner flames to invert and increasing fire risk. Dealers will inspect and seal it free of charge.
Product
KEYSTONE — KEYSTONE COUGAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V300000·2020-05-23
AEV TraumaHawk Ambulances Recalled for Rear Brake Line Wear Risk
Halcore Group is recalling 2019-2020 AEV TraumaHawk ambulances because rear brake lines may wear from contact with suspension parts, risking brake loss.
Product
AEV — AEV TRAUMAHAWK
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·007-2020-EXP ·2020-05-22
Conagra Recalls Frozen Chicken and Turkey Bowls Due to Rock Contamination
Conagra Brands is recalling approximately 276,872 pounds of frozen Healthy Choice Power Bowls because they may contain small rocks. No illnesses have been reported.
Product
Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·20V298000·2020-05-22
Mercedes-Benz Recalls 2012 C-Class Vehicles for Incorrect Air Bag Replacement
Mercedes-Benz is recalling 2012 C-Class vehicles where an incorrect front passenger air bag may have been installed during a prior recall, potentially reducing crash protection.
Product
MERCEDES-BENZ — MERCEDES-BENZ C300, AMG C63, C250, C350
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V297000·2020-05-22
2020-2021 Forest River Surveyor Travel Trailers Safety Chain Recall
Forest River is recalling 2020-2021 Surveyor travel trailers because the safety chains are insufficient for the trailer's weight rating and may break if the trailer becomes unhitched, risking complete detachment.
Product
FOREST RIVER — FOREST RIVER SURVEYOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V299000·2020-05-22
Triple E Recalls 2020 Unity Travel Trailers Due to Latch Defect
Triple E is recalling 2020 Unity travel trailers because a latch may lock, blocking access to the propane shutoff valve and increasing fire risk.
Product
TRIPLE E — TRIPLE E UNITY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V296000·2020-05-22
KZRV Recalls 2018 Escape Trailers Due to Incorrect Tire Labels
KZRV is recalling 2018 Escape recreational trailers because incorrect tire labels may cause overinflation, increasing crash risk.
Product
KZRV — KZRV ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V294000·2020-05-21
Dennis Eagle Elite Garbage Trucks Recalled for Braking System Defect
Dennis Eagle is recalling 2017-2018 Elite garbage trucks because the anti-lock braking system may activate on the wrong side, increasing stopping distance.
Product
DENNIS EAGLE — DENNIS EAGLE ELITE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V295000·2020-05-21
2021 Chevrolet Trailblazer lacks tire size and pressure label information
General Motors is recalling certain 2021 Chevrolet Trailblazer vehicles with optional sport terrain tires because their certification labels do not show tire size and cold tire pressure information required by federal safety standards.
Product
CHEVROLET — CHEVROLET TRAILBLAZER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20746·2020-05-21
Viva Doria Recalls Wintergreen Essential Oil Due to Packaging Defect
Viva Doria is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Product
Viva Doria Wintergreen Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20747·2020-05-21
Herman Miller and Design Within Reach Recall Dressers and Cabinets for Tip-Over Hazards
Herman Miller and Design Within Reach are recalling Nelson and Lauki dressers and cabinets because they can tip over and entrap children. Consumers should stop using unanchored units and contact the company for a refund.
Product
Nelson and Lauki Dressers and Cabinets
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·20V286000·2020-05-20
Toyota Recalls 2019-2020 RAV4 Models for Front Suspension Arm Cracks
Toyota is recalling 2019-2020 RAV4 and RAV4 Hybrid vehicles because front lower suspension arms may crack and separate, risking loss of vehicle control.
Product
TOYOTA — TOYOTA RAV4, RAV4 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1932-2020·2020-05-20
Philips Zenition 50 Medical Device Recalled for Electrical Contact Failure
Philips is recalling 25 Zenition 50 devices because strain relief loss can cause electrical contacts to break, potentially exposing live parts or losing the video signal.
Product
Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V293000·2020-05-20
Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect
Vac-Tron is recalling 2016-2020 vacuum excavator trailers because the rear extends too far, failing federal safety standards and increasing crash risks.
Product
VAC-TRON — VAC-TRON CS 1270 GT, CS 870 GT, CS 873 GT, CV 1273 GT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1960-2020·2020-05-20
Intuitive Surgical Recalls da Vinci Xi Systems Due to Arm Faults
Intuitive Surgical is recalling 74 da Vinci Xi Surgical Systems because a manufacturing variation can cause arm faults and loss of functionality during surgery.
Product
da Vinci Xi Surgical System
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1945-2020·2020-05-20
Beckman Coulter iQ200 Urine Analyzer Recalled for Electrical Short Risk
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers due to a defect in the SATA power adapter cable that poses a risk of electrical short, charring, smoke, or flames.
Product
iQ200 Series Urine Microscopy Analyzer- All part numbers
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1944-2020·2020-05-20
Beckman Coulter iChem VELOCITY Urine Chemistry System Recalled for Fire Risk
Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Systems due to a defect in the SATA power adapter cable that poses a risk of electrical short, smoke, or flames.
Product
iChem¿VELOCITY Urine Chemistry System-
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V284000·2020-05-20
REV Recalls 2018-2020 Type 1 Ambulances for Rear Brake Line Wear
REV is recalling 2018-2020 Type 1 ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
Product
FRONTLINE — FRONTLINE, ROAD RESCUE, WHEELED COACH TYPE I
Category
Vehicle
Distribution
Distributed nationwide