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.

38951–38975 of 82058

  • SevereFDA (Drugs)·D-0732-2019·2019-03-20

    King Bio Recalls Anti-Aging Cream Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955714729, NDC 57955-7148-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0557-2019·2019-03-20

    King Bio Recalls Homeopathic Arnica Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Advanced Arnica due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Advanced Arnica, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955598428, NDC 57955-5984-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1006-2019·2019-03-20

    FDA Recalls NexGen Trabecular Metal Tibial Augments Due to Labeling Mismatch

    Zimmer Trabecular Metal Technology is recalling 26 units of NexGen Trabecular Metal Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800436 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19730·2019-03-20

    Kubota Recalls Zero Turn Mowers Due to Fire Hazard

    Kubota is recalling about 3,850 zero turn mowers because the throttle cable can contact internal wiring, posing a fire hazard. No injuries have been reported.

    Product
    Kubota Zero Turn Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V221000·2019-03-20

    Osage Ambulances Recalled for Brake Lights Illuminating Without Pedal Press

    Osage is recalling 2015-2019 Brave, Warrior, and Super Warrior ambulances because brake lights may illuminate when the brake pedal is not pressed, potentially confusing other drivers.

    Product
    OSAGE — OSAGE BRAVE, WARRIOR, SUPER WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19088·2019-03-20

    Honda Recalls Portable Generators Due to Fire and Burn Hazards

    American Honda is recalling approximately 200,000 portable generators because a fuel valve leak can cause fire and burn hazards. No injuries have been reported.

    Product
    Honda EU2200i, EU220i Companion and EB2200i Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0994-2019·2019-03-20

    Durex Pleasure Pack Condoms Recalled for Burst Pressure Failure

    Reckitt Benckiser is recalling Durex Pleasure Pack condoms because five batches failed burst pressure specifications.

    Product
    Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1167-2019·2019-03-20

    Nature's Path Organic Chocolate Choco Chimps Cereal Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Chocolate Choco Chimps cereal because it may contain undeclared gluten (wheat and barley).

    Product
    Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt. 10 oz (284 g), UPC 58449-87024. Nature's Path Foods, Inc., Blaine, WA 98230
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1156-2019·2019-03-20

    Finax Muesli Recalled for Unlabeled Hazelnut Allergen

    Chicago Importing Co is recalling Finax Muesli with Nuts and Fruit because the product was mislabeled and contains hazelnuts not listed on the label.

    Product
    Finax Muesli with Nuts and fruit 22.9-oz. Heat sealed plastic bag; 10 bags/case UPC: 7311142201402
    Category
    Food
    Distribution
    11 states
  • HighNHTSA·19V218000·2019-03-20

    Volkswagen Atlas and Passat Recall for Incorrect Side Air Bags

    Volkswagen is recalling 2019 Atlas and 2020 Passat vehicles because incorrect side air bags may have been installed, potentially failing to deploy in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0993-2019·2019-03-20

    Durex Real Feel Condoms Recalled for Burst Pressure Failure

    Reckitt Benckiser LLC is recalling Durex Real Feel condoms because five batches failed burst pressure specifications.

    Product
    Durex Real Feel, synthetic polisoprene male condom, SKU 02340-89456-14 02340-89455-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-95767-00 02340-89456-14 02340-89457-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-89455-00 02340-95767-00 02340-95767-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V215000·2019-03-20

    Thor Motor Coach Recalls 2018-2019 Quantum RW28 Motorhomes for Missing Lights

    Thor Motor Coach is recalling 2018-2019 Quantum RW28 motorhomes because they may be missing mid-ship marker lights, which can cause other drivers to underestimate the vehicle's length.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0996-2019·2019-03-20

    Steris Recalls AMSCO 5000 Series Washer/Disinfector Units Due to Software Defect

    Steris Corporation is recalling 68 AMSCO 5000 Series Washer/Disinfector units because a software defect may prevent the intended cleaning cycle from processing, potentially leading to inadequate disinfection.

    Product
    AMSCO 5000 Series Washer/Disinfector Model # 5052
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Food)·F-1168-2019·2019-03-20

    Nature's Path Organic Gorilla Munch Corn Puffs Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Gorilla Munch Corn Puffs cereal because it may contain undeclared gluten (wheat and barley). The recall covers 23,969 cases distributed nationwide and internationally.

    Product
    Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g), UPC 58449-86002. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V214000·2019-03-20

    Fouts Bros Fire Apparatus Recall for Brake Light Wiring Defect

    Fouts Bros is recalling 2017-2018 F-3000, F-Rescue, and F-Pumper fire apparatus vehicles because brake lights may illuminate without the brake pedal being pressed.

    Product
    FOUTS BROS. — FOUTS BROS. F-PUMPER, F-3000, F-RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1169-2019·2019-03-20

    Nature's Path Organic Cinnamon Jungle Munch Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Cinnamon Jungle Munch cereal because it may contain undeclared gluten (wheat and barley).

    Product
    Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g), UPC 58449-87028. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1011-2019·2019-03-20

    US Endoscopy Padlock Clip Recalled for Potential Esophageal Laceration Risk

    US Endoscopy Group Inc is recalling Padlock Clip defect closure systems due to a risk of esophageal laceration during patient procedures.

    Product
    US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0995-2019·2019-03-20

    Steris Recalls AMSCO 3000 Series Washer/Disinfector Units Due to Software Defect

    Steris Corporation is recalling 11 AMSCO 3000 Series Washer/Disinfector units because a software defect may prevent intended processing cycles, risking inadequate cleaning or damage to medical instruments.

    Product
    AMSCO 3000 Series Washer/Disinfector Model # 3052
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-1010-2019·2019-03-20

    Olympus TJF-Q180V Duodenoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling two TJF-Q180V duodenoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the device's durability or effectiveness.

    Product
    Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1003-2019·2019-03-20

    Ossur ReSolve Halo Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 381 ReSolve Halo Vests because the titanium pin label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur, ReSolve Halo Vest, Part/ Description: 545700K/ ReSolve Halo Vest-shrt kodel; 545700L/ ReSolve Halo Vest-shrt lmbwool; 545800K/ ReSolve Halo Vest-tall kodel; 545800L/ ReSolve Halo Vest-tall lmbwool
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1000-2019·2019-03-20

    Ossur CB Resolve Halo System Recalled for Labeling and Testing Issues

    Ossur Americas is recalling 656 units of CB Resolve Halo system products due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur CB Resolve, Sterile, Part/ Description: 505300C/ CB RESOLVE STERILE UNIT SML; 505400C/ CB RESOLVE STERILE UNIT STD; 505500C/ CB Resolve Sterile Unit LRG; 515300C/ CB RESOLVE RING KIT SM-No App; 515400C/ CB RESOLVE RING KIT STD-No App; 515500C/ CB RESOLVE RING KIT…
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1009-2019·2019-03-20

    Olympus PCF-Q180AC Video Colonoscope Recalled Due to Adhesive Error

    Olympus is recalling two video colonoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the durability of the repair.

    Product
    Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0996-2019·2019-03-20

    Lannett Recalls Oxybutynin Chloride Tablets for Dissolution Failures

    Lannett Company Inc. is recalling 14,448 bottles of Oxybutynin Chloride Extended-Release Tablets because they failed to meet dissolution specifications.

    Product
    OXYBUTYNIN CHLORIDE — OXYBUTYNIN CHLORIDE (OXYBUTYNIN CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1004-2019·2019-03-20

    Ossur LIL Angel Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 45 LIL Angel Vests because the titanium pin labels incorrectly list ceramic tips and require confirmatory safety testing.

    Product
    Ossur, LIL Angel Vest, Part/ Description: 545100K/ LIL ANGEL VEST P2 KODEL; 545100L/ LIL ANGEL VEST P2 LAMBSWOOL; 545100S/ LIL ANGEL VEST P2 SORBATEX; 545150K/ LIL ANGEL VEST P3 KODEL; 545150L/ LIL ANGEL VEST P3 LAMBSWOOL; 545150S/ LIL ANGEL VEST P3 SORBATEX
    Category
    Medical Device
    Distribution
    28 states