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.

48501–48525 of 82079

  • ModerateFDA (Food)·F-2234-2017·2017-05-24

    Kemps Recalls Sweet Me Creamery Ice Cream and Frozen Yogurt for Plastic

    Kemps, LLC is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.

    Product
    Kemps Sweet Me Creamery Maple Toffee Blondie, One Pint, UPC 41483-04146
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-2239-2017·2017-05-24

    Herbalife Recalls Peanut Butter Protein Bars Due to Fish Gelatin

    Herbalife is recalling Peanut Butter Protein Bars because they may contain trace amounts of fish gelatin, an undeclared allergen.

    Product
    Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each shipping carton contains 12 boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0790-2017·2017-05-24

    Taro Recalls Fluocinonide Cream Due to Hydrocortisone Contamination

    Taro Pharmaceuticals is recalling specific lots of Fluocinonide Cream 0.05% due to cross-contamination with hydrocortisone-17-valerate.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2104-2017·2017-05-24

    Medline Recalls Distraction Pins Due to Potential Sterility Loss

    Medline Industries is recalling 2,112 packs of sterile distraction pins because the packaging seal may be compromised, risking loss of sterility.

    Product
    16 mm [or 18 mm] Distraction Pin, Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2017·2017-05-24

    Medline 12 mm Distraction Pin Recalled for Potential Sterility Loss

    Medline Industries is recalling 300 packs of 12 mm Distraction Pins because the sterile packaging seal may be compromised, potentially allowing the device to lose sterility.

    Product
    12 mm Distraction Pin, Blunt Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2108-2017·2017-05-24

    Teleflex Recalls Visistat Skin Staplers Due to Labeling Error

    Teleflex Medical is recalling Visistat 35R Disposable Skin Staplers because some boxes are mislabeled as containing Wide devices when they contain Regular devices.

    Product
    WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic, cardiovascular…
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-2090-2017·2017-05-24

    Hitachi Arietta 70 Ultrasound System Recalled for Weak Arm Mounting Mechanism

    Hitachi Medical Systems America Inc is recalling 77 Arietta 70 Ultrasound Systems because the arm mounting mechanism was insufficiently strong and required redesign.

    Product
    Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic Ultrasound evaluation.
    Category
    Medical Device
    Distribution
    18 states
  • LowFDA (Devices)·Z-2116-2017·2017-05-24

    Medtest Holdings Recalls Pointe Scientific Hitachi AST Reagent Due to Labeling Discrepancy

    Medtest Holdings is recalling Pointe Scientific Hitachi AST Reagent because the package insert contains inconsistent linearity values in different sections.

    Product
    Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle w/PP plastic cap. R2: PE plastic bottle w /PP plastic cap. Product Usage: Two Part Chemistry Reagent For the quantitative determination of Aspartate Aminotransferase (ASl) in human serum on Hitachi analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17164·2017-05-23

    Pier 1 Imports Recalls Temani Wicker Furniture for Lead Paint Violation

    Pier 1 Imports is recalling Temani wicker chairs, settees, and ottomans because the paint may contain excessive lead, violating federal standards.

    Product
    Temani ivory wicker chair, settee and ottoman
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17166·2017-05-23

    Hobby Lobby Recalls Easter and July 4th Light-Up Spinner Toys

    Hobby Lobby is recalling Easter and July 4th-themed light-up spinner toys because the battery cover can detach, exposing coin cell batteries that pose choking and ingestion hazards to young children.

    Product
    Easter and July 4th-themed Light-Up Spinner Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V334000·2017-05-23

    REV Road Rescue Emergency Vehicles Recalled for Cot Securing Bolt Defect

    REV is recalling 24 Road Rescue emergency vehicles because short bolts may fail to secure the cot during a crash, potentially injuring occupants.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE I, TYPE IX, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V335000·2017-05-23

    Keystone Recalls 2017-2018 Dutchmen Voltage Trailers Due to Fuel Line Defect

    Keystone RV Company is recalling 2017-2018 Dutchmen Voltage trailers with Onan 5.5 generators because an incorrectly clamped fuel line may disconnect, causing a fuel leak and fire risk.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17162·2017-05-23

    Dynacraft Recalls Ride-On Toys Due to Sticking Pedal Hazard

    Dynacraft is recalling about 20,000 Surge and Tonka battery-operated ride-on toys because the acceleration pedal can stick, posing fall and crash hazards.

    Product
    Surge and Tonka battery operated ride-on toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17T010000·2017-05-23

    Kenda Kenetica Tires Recalled for Steel Belt Void Risk

    American Kenda Rubber Industrial is recalling specific Kenetica tires due to a void in the steel belt that may cause tread separation or sudden air loss.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V331000·2017-05-22

    Ford Recalls 2015-2017 F-Series Trucks for Door Handle Cover Defect

    Ford is recalling specific 2015-2017 F-Series trucks equipped with chrome door handle covers that may cause doors to unlatch in a side impact, increasing injury risk.

    Product
    FORD — FORD F-150, redundant F-350, redundant F-250, F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V332000·2017-05-22

    Ford Recalls 2017 Models for Manual Seat Recliner Weld Defect

    Ford is recalling 2017 Explorer and F-Series trucks because manual seat back recliners may have inadequate welds, increasing injury risk in a crash.

    Product
    FORD — FORD EXPLORER, F-150, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V333000·2017-05-22

    Harley-Davidson Recalls 2017 Motorcycles Due to Oil Cooler Line Clamp Defect

    Harley-Davidson is recalling 45,589 2017 motorcycles because an improperly installed clamp may cause the engine oil cooler line to detach, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCU, FLTRX, FLHTP, FLHRXS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-051617-exp·2017-05-20

    Imported Veal Products Recalled Over Possible E. coli O103 Contamination

    USDA FSIS issued a Public Health Alert for approximately 1,631 pounds of raw veal products imported from the Netherlands due to possible contamination with Non-O157 Shiga toxin-producing E. coli O103. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert For Imported Veal Products Due To Possible Non-O157 Shiga toxin producing E. coli (STEC) O103 Contamination
    Category
    Food
    Distribution
    4 states
  • CriticalCPSC·17159·2017-05-19

    Blomberg and Summit Electric Ranges Recalled for Electrocution Hazard

    Arçelik A.S. is recalling about 6,300 Blomberg and Summit electric ranges because they can become energized, posing shock and electrocution risks.

    Product
    Blomberg and Summit electric ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V330000·2017-05-19

    Columbia Aliner Ascape Trailers Recalled for Loose Propane Gas Trays

    Columbia Northwest is recalling 2017-2018 Aliner Ascape trailers because liquid propane gas bottle trays may detach, increasing the risk of fire or crash.

    Product
    COLUMBIA — COLUMBIA ALINER ASCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide