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.

46926–46950 of 82079

  • HighFDA (Food)·F-2893-2017·2017-08-02

    ICYBAY Raw Breaded Flounder Fillets Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling ICYBAY Raw Breaded Natural Flounder Fillets due to undeclared milk. The product was distributed to 14 states.

    Product
    ICYBAY - Raw Breaded Natural Flounder Fillets Approx - 5OZ NET WT. 10LBS (4.54Kg)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2919-2017·2017-08-02

    ICYBAY Raw Breaded Pollock Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling ICYBAY Raw Breaded AK Pollock Square due to undeclared milk. The product was distributed to 14 states.

    Product
    ICYBAY - Raw Breaded AK Pollock Square 4OZ - NET WT. 10 LBS. (4.54Kg)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2934-2017·2017-08-02

    Checkers/Rally's Fish Breaded Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling Checkers/Rally's Fish Breaded due to undeclared milk. The product was distributed to 14 states.

    Product
    Checkers/Rally's Fish Breaded 2.5oz, 120-128 Count, Net Wt. 20 LBS
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2899-2017·2017-08-02

    Channel Brand Raw Breaded Haddock Tails Recalled for Undeclared Milk

    Channel Fish Processing Co. Inc. is recalling raw breaded haddock tails because they contain undeclared milk, a major food allergen.

    Product
    Channel Brand - 4oz. Raw Breaded Haddock Tails Net wt. 10lb (4.54 KG)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2763-2017·2017-08-02

    Fisher Diagnostics Recalls FDP Latex Reagent Due to Reduced Sensitivity

    Fisher Diagnostics is recalling specific lots of Pacific Hemostasis FDP Latex Reagent because reduced sensitivity may cause false negative test results.

    Product
    Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company, LLC, a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2915-2017·2017-08-02

    Channel Brand Panko Breaded Tilapia Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling Channel Brand Panko Breaded Tilapia because the product contains undeclared milk, a major food allergen.

    Product
    Channel Brand - 1-3 oz Panko Breaded Tilapia - Net Wt. 10 lbs. (4.54 kg)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2767-2017·2017-08-02

    Medtronic Recalls DLP Pressure Monitoring Extension Line Adapters

    Medtronic Perfusion Systems is recalling DLP Pressure Monitoring Extension Line Adapters due to small pinholes in sterile packaging.

    Product
    DLP Pressure Monitoring Extension Line Adapters Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2932-2017·2017-08-02

    Channel Fish Processing Recalls Raw Breaded Flounder Tails for Undeclared Milk

    Channel Fish Processing Co. Inc. is recalling raw Oriental Breaded Fish Portions due to undeclared milk. The product was distributed to 14 states.

    Product
    Winsor Bay - Raw Oriental Breaded Fish Portions - 4 oz. Flounder Tails - Net Wt. 10 lbs (4.54 KG)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2904-2017·2017-08-02

    Channel Brand Raw Breaded Cod Tails Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Cod Tails due to undeclared milk. The product was distributed to 14 states.

    Product
    Channel Brand - 5oz. Raw Breaded Cod Tails - Net Wt. 10 lb. (4.54 KG)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2911-2017·2017-08-02

    Channel Brand Raw Breaded Haddock Cuts Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Haddock Cuts because the product contains undeclared milk, a major food allergen.

    Product
    Channel Brand - 2-3oz. Raw Breaded Haddock Cuts - Net wt. 10 lbs. (4.54 kg)
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-2920-2017·2017-08-02

    Channel Brand Raw Breaded Pollock Squares Recalled for Undeclared Milk

    Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Pollock Squares due to undeclared milk. The product was distributed to 14 states.

    Product
    Channel Brand - 4OZ Raw Breaded Pollock Squares - Net wt.10 lbs. (4.54 kg) Channel Brand- 4 oz. Raw Breaded Pollock Squared Net Wt. 10 lb. (4.54 KG)
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-2765-2017·2017-08-02

    Medtronic DLP Antegrade/Retrograde Adapter Recalled for Packaging Pinholes

    Medtronic is recalling DLP Antegrade/Retrograde Adapters because small pinholes were found in a single packaging configuration of sterile pouches.

    Product
    DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with flexible lines and standard luer sites to facilitate direct connections to the cannulae
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2927-2017·2017-08-02

    Channel Fish Processing Recalls Raw Breaded Whiting Squares for Undeclared Milk

    Channel Fish Processing Co. Inc. is recalling raw breaded whiting squares because the product contains milk, which is not declared on the label.

    Product
    PRIMA - 3 OZ Raw Breaded Whiting Squares - NET WT 10 LBS. (4.54 KG.) PRIMA - 4 OZ Raw Breaded Whiting Squares - NET WT 10 LBS. (4.54 KG.)
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-2898-2017·2017-08-02

    Channel Fish Processing Recalls Raw Breaded Fish Portions for Undeclared Milk

    Channel Fish Processing Co. Inc. is recalling raw Oriental Breaded Fish Portions due to undeclared milk. The product was distributed to 14 states.

    Product
    Winsor Bay- Raw Oriental Breaded Fish Portions - 4 oz. Haddock Tails - Net wt. 10 lbs (4.54.KG)
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-2768-2017·2017-08-02

    Medtronic Recalls DLP Pressure Display Sets Due to Packaging Pinholes

    Medtronic Perfusion Systems is recalling DLP Pressure Disposable Pressure Display Sets because small pinholes were found in the sterile packaging.

    Product
    DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2761-2017·2017-08-02

    Atrium iCAST and Advanta V12 Stents Recalled for Incorrect Hub Labeling

    Atrium Medical Corporation is recalling specific iCAST and Advanta V12 covered stents because the catheter hub was printed with incorrect dimensional information.

    Product
    Atrium iCAST Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85455 (Marketed in U.S. only) Atrium Advanta V12 Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85355 (Marketed OUTSIDE U.S. only) The iCAST Covered Stent is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2766-2017·2017-08-02

    Medtronic Recalls DLP Cardioplegia Adapters Due to Packaging Pinholes

    Medtronic Perfusion Systems is recalling DLP Cardioplegia Adapters with Pressure Port because small pinholes were identified in a single packaging configuration of sterile pouches.

    Product
    DLP Cardioplegia Adapter with Pressure Port Provides access for a pressure monitoring needle near the connection to the cardioplegia cannula. These adapters are intended for use in conjunction with the delivery of cardioplegia solution and to provide access for pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2757-2017·2017-08-02

    Cardinal Health Recalls Mislabeled Sterile Surgical Drapes

    Cardinal Health is recalling specific lots of sterile surgical drapes because the outer labels do not match the packaged product inside.

    Product
    Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2758-2017·2017-08-02

    Cardinal Health Recalls Tiburon Arthroscopy Drapes Due to Labeling Mismatch

    Cardinal Health is recalling specific lots of Tiburon Arthroscopy Drapes because the outer labels do not match the packaged product.

    Product
    Converters(R) Tiburon(R) Arthroscopy Drape, REF 9414, STERILE EO, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E042000·2017-08-01

    Timken Recalls Rear Hub Unit Bearings for Ford Explorers

    Timken is recalling specific rear hub unit bearings for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.

    Product
    SUSPENSION:REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide