The Recall Desk

State

Massachusetts product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51376–51400 of 82085

  • CriticalFDA (Devices)·Z-0307-2017·2016-11-16

    FDA Recalls Pipeline Embolization Devices Due to Coating Delamination

    Micro Therapeutics Inc is recalling Pipeline Embolization Devices because PTFE coating may delaminate and enter the bloodstream.

    Product
    Pipeline Embolization Device (Pipeline Classic) The device is indicated for the endovascular treatment of adults (22 year of age or older) with large or giant widenecked intracranial aneurysms (lAs) in the internal carotid artery from the petrous to the superior hypophyseal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0310-2017·2016-11-16

    Ev3 Neurovascular Recalls X-Celerator Hydrophilic Exchange Guidewires

    Micro Therapeutics Inc is recalling X-Celerator Hydrophilic Exchange Guidewires because PTFE coating delamination may release material into the bloodstream.

    Product
    X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0351-2017·2016-11-16

    Professional Botanicals Recalls MealPlex and Pearl Drinks for Undeclared Milk

    Professional Botanicals is recalling specific lots of MealPlex and Pearl meal drinks because they contain undeclared milk, a major food allergen.

    Product
    Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0 (378 grams) Ultimate Meal Drinks in Plastic Tub Containers. Dietary Supplement.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0374-2017·2016-11-16

    Siemens SOMATOM Definition Flash CT Systems Recalled for Injury Risk

    Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition Flash system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0373-2017·2016-11-16

    Siemens SOMATOM Definition AS CT Systems Recalled for Injury Risk

    Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition AS system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0325-2017·2016-11-16

    On the Border Tortilla Chips Recalled for Possible Metal Fragments

    Truco Enterprises is recalling On the Border Cafe Style Tortilla Chips due to possible metal fragments in the corn flour.

    Product
    On the Border Cafe Style Tortilla Chips 18 oz. and 28 oz. packaged in laminated polypropylene film with windows.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0378-2017·2016-11-16

    Stryker Recalls LFIT Anatomic V40 Femoral Heads Due to Taper Lock Failure

    Stryker Howmedica Osteonics is recalling specific lots of LFIT Anatomic V40 Femoral Heads because of reported taper lock failures that caused harm.

    Product
    LFIT Anatomic V40 Femoral Head, Low Friction Ion Treatment, Sterile, 36 mm, REF 6260-9-236; Modular components designed to be locked onto a femoral hip stem trunnion during surgery for total hip replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0309-2017·2016-11-16

    Ev3 Neurovascular Recalls Marathon and UltraFlow Micro Catheters

    Micro Therapeutics Inc. is recalling Marathon and UltraFlow HPC Flow Directed Micro Catheters because PTFE coating may delaminate and enter the bloodstream.

    Product
    Marathon Flow Directed Micro Catheter, UltraFlow HPC Flow Directed Micro Catheter Marathon Flow: The device is intended to access periphera and neurovasculature for the controlled selective infusion of physician-specified therapeutics agents such as embolization materials and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0390-2017·2016-11-16

    Maquet Accessory Adapter Recalled Due to Head Rest Slipping Hazard

    Maquet Medical Systems USA is recalling Accessory Adapter part number 600525A0 because a head rest mounted to the device slipped out of the mounting rail.

    Product
    Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail guide interface immediately before, during and after surgical interventions as well as for examination and treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0362-2017·2016-11-16

    Hospira Symbiq Infusion Pump Recall for White Screen Safety Shutdown

    Hospira is recalling Symbiq Two Channel Infusers that may display a white screen, causing the device to stop infusion and sound an alarm, which can delay or interrupt therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List number 16027. Note that Hospira retired this pump June 30, 2015. The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0285-2017·2016-11-16

    Koffee Kup Hamburger Buns Recalled for Plastic Contamination

    Koffee Kup Bakery is recalling hamburger buns in multiple states due to potential plastic pieces.

    Product
    Koffee Kup Hamburger Buns- White, Wheat, Seeded -3 1/2" 4", 5", packaged 16 oz. 18, oz, 20 oz, 25 oz, 29 oz
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0427-2017·2016-11-16

    Sokol and Co Recalls Solo Almond Paste Due to Foreign Material

    Sokol and Co is recalling Solo Almond Paste because pieces of plastic and metal were discovered in the product. The recall affects 486 cans distributed in Massachusetts, Michigan, and Texas.

    Product
    Solo Almond Paste, 6/7 LB. Cans, Net Weight: 42 LBS. (19.09 KG.)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0391-2017·2016-11-16

    Trumpf Medical Systems Recalls Operating Room Table Tops for Cable Pinching

    Trumpf Medical Systems is recalling specific operating room table tops after identifying six incidents of pinched cables.

    Product
    OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794; OR Table Top U24 H V, Model # 1909796; OR Table Top U24 H V U, Model # 1909797; OR Table Top U24 H V W, Model # 1909798; OR Table Top U14 H V, Model # 1909799 Product Usage: Patient positioning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0288-2017·2016-11-16

    Koffee Kup Hot Dog Buns Recalled for Plastic Contamination

    Koffee Kup Bakery Inc. is recalling hot dog buns because they may contain plastic pieces. Consumers should stop eating the product.

    Product
    Koffee Kup Hot Dog Buns- 8 pk and 16 pk
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0370-2017·2016-11-16

    Baxter Recalls Revaclear MAX Dialyzers Due to Potential Particulate Matter

    Baxter Healthcare is recalling 22,656 Revaclear MAX dialyzers because of potential particulate matter on the blood side of the device.

    Product
    GAMBRO Capillary Dialyzer, Polyflux(R) Revaclear MAX, STERILE, Product code 110634 Product Usage: The Revaclear Max dialyzer is a single use device used for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0361-2017·2016-11-16

    Hospira Symbiq Infusion Pump Recalled for White Screen Shutdown

    Hospira is recalling 10,337 Symbiq One Channel Infusers because a software issue may cause a white screen, stopping infusion and interrupting therapy.

    Product
    Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List number 16026. Note that Hospira retired this pump June 30, 2015. The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0284-2017·2016-11-16

    Koffee Kup Bakery Recalls Hoogie Rolls Due to Plastic Contamination

    Koffee Kup Bakery Inc. is recalling Hoogie Rolls in various flavors and sizes because they may contain pieces of plastic.

    Product
    Koffee Kup Hoogie Rolls- Wheat, Sourdough, Potatoe packaged 15 oz and 15.6 and 17 oz
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0377-2017·2016-11-16

    AtriClip LAA Exclusion System Recalled for Potential Component Failure

    AtriCure, Inc. is recalling 298 AtriClip LAA Exclusion Systems due to a potential component failure that could require medical intervention.

    Product
    AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's left atrial appendage, under direct visualization, in conjunction with other open cardiac surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17033·2016-11-16

    Skidders Recalls Children's Shoes Due to Sharp Rivet Laceration Hazard

    Skidders Footwear is recalling about 5,500 children's canvas tennis shoes because sharp rivets pose a laceration hazard. Consumers should take shoes away from children and contact the company for a refund.

    Product
    Children's shoes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0423-2017·2016-11-16

    Brownwood Farms Cherry Butter Recalled for Undeclared Milk Allergen

    Brownwood Farms is recalling Cherry Butter products because they contain milk that is not declared on the label.

    Product
    Brownwood Farms America's Original Cherry Butter 12oz and 22oz glass bottles and 1 gallon. Private labels: Arbor Day Farm (Cherry Butter 12oz). Bowers Harbor Vineyards (Cherry Butter 12oz). Crossroads (10oz). Central Market (16oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0420-2017·2016-11-16

    Brownwood Farms Cherry Raspberry Preserves Recalled for Undeclared Milk

    Brownwood Farms is recalling Cherry Raspberry Preserves because the product contains milk that is not declared on the label.

    Product
    Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0422-2017·2016-11-16

    Brownwood Farms Jalapeno Cherry Butter Recalled for Undeclared Milk

    Brownwood Farms is recalling Jalapeno Cherry Butter products because they contain milk that is not declared on the label.

    Product
    Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Jalapeno Cherry Butter 12oz). Benjamin Twiggs (Cherry Pepper Jam 10oz). Central Market (16oz).
    Category
    Food
    Distribution
    Distributed nationwide