The Recall Desk

State

Massachusetts product recalls

73,827 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.

These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47651–47675 of 82079

  • SevereNHTSA·17V413000·2017-06-29

    Newmar Recalls 2018 Motorhomes Due to Fuel Pump Drive Gear Slip Risk

    Newmar is recalling 2018 London Aire, King Aire, and Essex motorhomes because a fuel pump drive gear could slip, causing an engine stall and increasing crash risk.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V412000·2017-06-29

    GM Recalls 2016-2017 Buick Envision for Headliner Safety Defect

    General Motors is recalling 2016-2017 Buick Envision vehicles because replacement headliners may lack required impact-absorbing foam, increasing injury risk in crashes.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V415000·2017-06-29

    Lexus Recalls 2017 ES350 Vehicles Due to Steering Tie Rod Defect

    Toyota is recalling 2017 Lexus ES350 vehicles because the right-hand tie rod lock nut may loosen, potentially causing loss of steering and increasing crash risk.

    Product
    LEXUS — LEXUS ES350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V429000·2017-06-29

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Mazda is recalling 2007-2011 CX-7, CX-9, and 2009-2011 Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V417000·2017-06-29

    Honda Recalls 2007-2011 CR-V Vehicles for Air Bag Inflator Defect

    Honda is recalling 2007-2011 CR-V vehicles where the passenger air bag inflator may have an incorrect wire harness, potentially preventing deployment in a crash.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V414000·2017-06-29

    GM Recalls 2014 Chevrolet Silverado and GMC Sierra for Steering Assist Loss

    General Motors is recalling 2014 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because they may experience a temporary loss of electric power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V416000·2017-06-29

    Toyota Recalls 2016 Tundra Vehicles Due to Passenger Knee Air Bag Bolt Issue

    Toyota is recalling 2016 Tundra vehicles because incorrect bolts were used to attach the passenger knee air bag module, which may loosen over time and affect air bag performance during a crash.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·17182·2017-06-28

    South Shore Recalls 5-Drawer Chests Due to Tip-Over Hazard

    South Shore Industries is recalling about 68,300 Summer Breeze style 5-drawer chests because they are unstable and can tip over if not anchored to the wall. Consumers should stop using the chests until they are secured or contact the company for a refund or free restraint kit.

    Product
    5-drawer chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2224-2017·2017-06-28

    Vascular Solutions Recalls Venture Catheters Due to Material Detachment Risk

    Vascular Solutions, Inc. is voluntarily recalling Venture RX, OTW, and CS catheters because material may detach from the distal tip during use.

    Product
    Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using ethylene oxide, Rx Only. The Venture catheter is indicated for directing, steering, controlling, and supporting a guidewire to access discrete regions of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2616-2017·2017-06-28

    DePuy Mitek LATARJET Coracoid Drill Recalled for Breakage Risk

    DePuy Mitek is recalling LATARJET Coracoid Drills because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • SevereNHTSA·17V410000·2017-06-28

    Lakota Colt Trailers Recalled Due to Furnace Venting Defect

    Lakota Corporation is recalling 2018 Colt trailers because the furnace flue may be improperly installed, preventing proper venting. This defect can cause carbon monoxide buildup inside the trailer, posing a risk of injury or death.

    Product
    LAKOTA — LAKOTA COLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2617-2017·2017-06-28

    DePuy Mitek LATARJET Drill Tip Recall Due to Breakage Risk

    DePuy Mitek is recalling LATARJET Coracoid Top Hat Drills because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0922-2017·2017-06-28

    Vi-Jon Recalls Magnesium Citrate Saline Laxative Due to Glass Particles

    Vi-Jon, Inc. is recalling 52,212 bottles of Magnesium Citrate Saline Laxative because glass particles were found in the product.

    Product
    Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17752·2017-06-28

    Homestar Recalls Three-Drawer TV Chests Due to Tip-Over Hazards

    Homestar North America is recalling about 1,470 Stockholm three-drawer TV chests sold at Target.com because they pose serious tip-over and entrapment hazards to children if not anchored to the wall.

    Product
    Stockholm three-drawer TV chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2619-2017·2017-06-28

    DePuy Mitek LATARJET Extraction Driver Recalled for Breakage Risk

    DePuy Mitek is recalling 115 units of the LATARJET EXPERIENCE Extraction Driver because the tip may break during surgery when used at an angle.

    Product
    DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2618-2017·2017-06-28

    DePuy Mitek Top Hat Tap Screw Driver Tip Recall

    DePuy Mitek is recalling 153 units of the LATARJET EXPERIENCE Top Hat Tap because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·17V409000·2017-06-28

    KME Predator Tanker Recalled for Fuel Pump Drive Gear Slip

    Kovatch Mobile Equipment is recalling one 2017 KME Predator Tanker truck because a fuel pump drive gear may slip, causing an engine stall that increases crash risk.

    Product
    KME — KME PREDATOR TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2592-2017·2017-06-28

    Ion Beam Applications Recalls Proteus 235 Medical Devices

    Ion Beam Applications S.A. is recalling 18 Proteus 235 systems due to potential dark current issues in Pencil Beam Scanning mode.

    Product
    Proteus 235
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2615-2017·2017-06-28

    DePuy Mitek LATARJET Combo Screw Driver Recalled for Breakage Risk

    DePuy Mitek is recalling 173 LATARJET Combo Screw Drivers because the tip may break during surgery when used at an angle.

    Product
    DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·17V407000·2017-06-28

    Lance Recalls 2018 Travel Trailers with Defective Utility Receivers

    Lance is recalling 2018 Travel Trailers with optional utility receivers that have insufficient welds, which may cause attached items to contact the road.

    Product
    LANCE — LANCE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2613-2017·2017-06-28

    Abbott Recalls ARCHITECT SHBG Reagent Due to Specimen Tube Interference

    Abbott Laboratories is recalling 7,981 kits of ARCHITECT SHBG Reagent because using Potassium EDTA specimen tubes may cause falsely decreased test results.

    Product
    ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative determination of sex hormone binding globulin (SHBG) in human serum and plasma on the ARCHITECT iSystem. The ARCHITECT SHBG assay is used as an aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide