The Recall Desk

State

Massachusetts product recalls

73,806 recalls have nationwide distribution and so reach Massachusetts. 8,252 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,252
Critical
1,179
Severe
2,360
Most recent
2026-11-04

Of the 8,252 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 2,360 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38426–38450 of 82058

  • HighFDA (Devices)·Z-1040-2019·2019-03-27

    Fujifilm FDR Go PLUS Mobile X-Ray System Recalled for Braking Defect

    Fujifilm is recalling 56 mobile X-ray systems because the braking mechanism may fail to engage when the handle is released.

    Product
    Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V240000·2019-03-27

    Thor Motor Coach Recalls 2018-2020 Models Due to Reversed Backup Camera Image

    Thor Motor Coach is recalling 110 motorhomes because the backup camera image may reverse, increasing crash risk. Dealers will install a harness to fix the issue.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS, CHATEAU, MAGNITUDE, OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2019·2019-03-27

    ConvaTec Recalls Feeding Tubes Due to Potential Sterile Barrier Breach

    ConvaTec is recalling specific lots of Feeding Tube Metric devices because an internal assessment found a potential breach in the sterile barrier.

    Product
    Feeding Tube Metric, disposable, sterile, 100 eaches per sales unit. Labeled as: xray CH05/40CM and xray CH08/40CM Product Usage: Duodenal and Stomach Gastroenterology Tubes are sterile disposable devices which may be inserted through the nose or mouth via the esophagus into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1019-2019·2019-03-27

    AAP Implantate Lambotte Chisel Recalled for Potential Breakage at Welded Parts

    AAP Implantate AG is recalling 25 units of the 20 mm Lambotte chisel due to a potential risk of breaking at the welded piece parts of the chisel body and knocking plate.

    Product
    aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1021-2019·2019-03-27

    Advanced Pharma Recalls Glycopyrrolate Syringes Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 2,580 syringes of Glycopyrrolate Injectable Solution nationwide due to a lack of assurance of sterility.

    Product
    Glycopyrrolate Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-828-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V243000·2019-03-27

    Osco Recalls Emergency Vehicles With Faulty Brake Light Wiring

    Osco Tank & Truck Sales is recalling 16,342 emergency vehicles built on 2012 Kenworth T440 and 2018 Peterbilt 348 chassis because brake lights may illuminate without the pedal being pressed.

    Product
    KENWORTH — KENWORTH, PETERBILT T440, 348
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V244000·2019-03-27

    Toyota Recalls 2019 Models Due to Illegible Load Capacity Labels

    Toyota is recalling specific 2019 models because the load capacity label text may become illegible, potentially leading to vehicle overload and increased crash risk.

    Product
    TOYOTA — TOYOTA CAMRY, AVALON, PRIUS, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V241000·2019-03-27

    Volkswagen Recalls 2019 Tiguan LWB for Inaccurate Tire Information Label

    Volkswagen is recalling 2019 Tiguan LWB vehicles because the tire information label contains inaccurate dimension and pressure specifications, which may increase crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1175-2019·2019-03-27

    Jansal Valley Chocolate Covered Almonds Recalled for Undeclared Sesame

    Friendly Fruit Market is recalling Jansal Valley Cocoa Dusted Chocolate Covered Almonds because the product contains undeclared sesame seeds.

    Product
    JANSAL VALLEY Cocoa Dusted Chocolate Covered Almonds, Net Weight: 6 OZ (170 G), packed in a plastic clamshell, UPC: 7 08152 32988 7
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1037-2019·2019-03-27

    ConvaTec Recalls Nelaton Urinary Catheters Due to Sterile Barrier Breach Risk

    ConvaTec is recalling Nelaton Urinary Catheters because an internal assessment found a potential breach in the sterile barrier, which could compromise the device's sterility.

    Product
    Nelaton Urinary Catheter, disposable, sterile, 100 eaches per sales unit. Labeled as: CH16/40CM and CH14/40CM Product Usage: Urinary Catheters are sterile disposable devices intended to provide an intermittent pathway for drainage of fluids from the bladder. They are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19091·2019-03-27

    Cambridge Elevating Recalls Home Elevators Due to Fall Hazard

    Cambridge Elevating is recalling approximately 680 home elevators because the landing door can unlock without the elevator present, posing a fall hazard.

    Product
    Home elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1027-2019·2019-03-27

    CP Medical Recalls Sterile Surgical Sutures Due to Potential Sterility Compromise

    CP Medical Inc is recalling Plain and Chromic Gut Absorbable Surgical Sutures because routine endotoxin testing showed an out-of-limit result, potentially compromising sterility.

    Product
    Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neural…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2019·2019-03-27

    FDA Recalls 850 Units of Covidien Force TriVerse Electrosurgical Devices

    The FDA is recalling 850 units of the Covidien Force TriVerse electrosurgical device due to potential sterile packaging compromise.

    Product
    Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1015-2019·2019-03-27

    Siemens Dimension Vista 1500 Analyzer Recall Due to Water Module Contamination

    Siemens is recalling 5,373 Dimension Vista 1500 analyzers because specific water purification modules may cause falsely elevated triglyceride results.

    Product
    Dimension Vista 1500, Analyzer, chemistry Model no. 10444801
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1033-2019·2019-03-27

    ACell Recalls Gentrix Surgical Matrix Thick Due to Tensile Strength Failure

    ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick because a sample failed to meet tensile strength specifications.

    Product
    Gentrix Surgical Matrix Thick, 20 x 30cm, Catalog Number PSMT2030, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1014-2019·2019-03-27

    Siemens Dimension Vista 500 Analyzer Recall for Water Module Contamination

    Siemens is recalling 5,373 Dimension Vista 500 analyzers because specific Millipore water purification modules may cause falsely elevated triglyceride results.

    Product
    Dimension Vista 500, Analyzer, chemistry Model no. 10284473
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1011-2019·2019-03-27

    Akorn Recalls Hydrocortisone and Acetic Acid Otic Solution Due to Low Potency

    Akorn Inc is recalling Hydrocortisone and Acetic Acid Otic Solution because routine stability testing revealed the drug was sub-potent.

    Product
    Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pharmacal Co, Inc., Amityville, NY 11701. NDC: 50383-901-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1038-2019·2019-03-27

    ConvaTec Recalls FilterFlow Suction Handles Due to Sterile Barrier Breach Risk

    ConvaTec is recalling 124,000 FilterFlow Suction Handles because an internal assessment found a potential breach in the sterile barrier.

    Product
    FilterFlow Suction Handle CH24, 20 eaches per sales unit. Product Usage: Filter Flow is designed for orthopedic surgery and combines suctioning function with filtering. The device is intended for orthopedic surgical procedures to remove and collect debris and bone fragments…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1035-2019·2019-03-27

    ConvaTec Recalls Forceps Blue Due to Potential Sterile Barrier Breach

    ConvaTec, Inc. is recalling Forceps Blue, disposable sterile forceps, because an internal assessment confirmed the potential for a breach in the sterile barrier.

    Product
    Forceps Blue, disposable, sterile, 100 eaches per sales unit. Product Usage: Forceps are sterile disposable devices intended for use during clinical procedures to grasp, manipulate, maneuver or assist with the removal of debris, particulates or wound tissue. Typically…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2019·2019-03-27

    ACell Recalls Gentrix Surgical Matrix Thick Due to Tensile Strength Failure

    ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick devices because a sample failed to meet tensile strength specifications.

    Product
    Gentrix Surgical Matrix Thick, 30 x 40cm, Catalog Number PSMT3040, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1024-2019·2019-03-27

    Cook Medical Recalls Celect Platinum Vena Cava Filters for Labeling Updates

    Cook Medical is recalling Celect Platinum Vena Cava Filter Sets to update the Instructions for Use. The recall affects 9,173 units distributed nationwide.

    Product
    Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach, Catalog Number IGTCFS-65-1-FEM-CELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1034-2019·2019-03-27

    Agfa Radiographic Film Recalled for Visible Pinholes in Images

    Agfa N.V. is recalling specific lots of PET Plates Coated Film-MONOMEDBV2S2 radiographic film because inhomogeneous coating solutions cause visible pinholes in images.

    Product
    PET Plates Coated Film-MONOMEDBV2S2- Radiographic Film REF: XJUB8, XJM73, XJUDD, XJM85, EKLYZ. Product Usage: Due to an inhomogeneous coating solution, pinholes can become visible in even dark images. Visibility of the pinholes varies as material from this coating run…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1026-2019·2019-03-27

    Cook Medical Recalls Celect Platinum Vena Cava Filters for Labeling Updates

    Cook Medical is recalling Celect Platinum Vena Cava Filter Sets to update the Instructions for Use. The recall affects 9,173 units distributed nationwide.

    Product
    Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-C ELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1023-2019·2019-03-27

    Cook Medical Recalls Gunther Tulip Vena Cava Filters for Labeling Updates

    Cook Medical is recalling 9,173 Gunther Tulip Vena Cava Filter Sets to update the Instructions for Use. The products were distributed nationwide.

    Product
    Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-TULIP Product Usage: The Gunther Tulip Filter is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following…
    Category
    Medical Device
    Distribution
    Distributed nationwide