The Recall Desk

State

Massachusetts product recalls

73,741 recalls have nationwide distribution and so reach Massachusetts. 8,248 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,248
Critical
1,179
Severe
2,356
Most recent
2026-10-28

Of the 8,248 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 2,356 (29%) are Severe.

These figures cover only the 8,248 recalls whose distribution notice names Massachusetts specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33876–33900 of 81989

  • SevereFDA (Drugs)·D-0719-2020·2020-01-22

    Assurance Infusion Recalls BUP 9MG/ HYDROM 25MG/ SUF 110MCG/ML INJ Syringes

    Assurance Infusion is recalling BUP 9MG/ HYDROM 25MG/ SUF 110MCG/ML INJ syringes due to a lack of sterility assurance.

    Product
    BUP 9MG/ HYDROM 25MG/ SUF 110MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0673-2020·2020-01-22

    Assurance Infusion Recalls Multi-Drug Syringes Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of a multi-drug injection syringe due to a lack of sterility assurance.

    Product
    BAC 400MCG/BUP 20MG/HYDROM 15MG/SUF 1000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0684-2020·2020-01-22

    Assurance Infusion Recalls BUP 15MG/CLON 400MCG/ FENT 6000MCG/ML INJ Syringes

    Assurance Infusion is recalling BUP 15MG/CLON 400MCG/ FENT 6000MCG/ML INJ in 20 mL syringes due to a lack of sterility assurance.

    Product
    BUP 15MG/CLON 400MCG/ FENT 6000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0760-2020·2020-01-22

    Assurance Infusion Recalls Morphine Injection Syringes Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of Morphine 6mg/mL injection syringes due to a lack of sterility assurance. The products were distributed nationwide.

    Product
    MORPHINE 6MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0741-2020·2020-01-22

    Assurance Infusion Recalls Hydromorphone Injection Due to Sterility Concerns

    Assurance Infusion is recalling Hydromorphone 1mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide in the United States.

    Product
    HYDROMORPHONE 1MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0774-2020·2020-01-22

    Assurance Infusion Recalls TRIMIX Injection Due to Sterility Assurance Concerns

    Assurance Infusion is recalling specific lots of TRIMIX injection due to a lack of sterility assurance. The product was distributed nationwide in the United States.

    Product
    TRIMIX (UA) 30MG/1MG/20MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0742-2020·2020-01-22

    Assurance Infusion Recalls Hydromorphone Injection Due to Sterility Concerns

    Assurance Infusion is recalling Hydromorphone 20mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.

    Product
    HYDROMORPHONE 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0661-2020·2020-01-22

    AvKARE Recalls Dutasteride Capsules Due to Impurity Specification Failures

    AvKARE Inc. is recalling specific lots of Dutasteride Capsules, 0.5 mg, because they failed impurity and degradation specifications.

    Product
    Dutasteride Capsules, 0.5 mg, 30 Capsules (6 X 5) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-282-13.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0754-2020·2020-01-22

    Assurance Infusion Recalls Morphine Syringes Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of Morphine 1mg/mL injection syringes due to a lack of sterility assurance. The affected products were distributed nationwide.

    Product
    MORPHINE 1MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0700-2020·2020-01-22

    Assurance Infusion Recalls BUP 30MG/HYDROM 10MG/ML Injection Due to Sterility Concerns

    Assurance Infusion is recalling BUP 30MG/HYDROM 10MG/ML Injection in 20 mL syringes due to a lack of sterility assurance. The recall covers products distributed nationwide in the United States.

    Product
    BUP 30MG/ HYDROM 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0732-2020·2020-01-22

    Assurance Infusion Recalls Fentanyl Injection Due to Sterility Concerns

    Assurance Infusion is recalling Fentanyl 5mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide in the United States.

    Product
    FENTANYL 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0764-2020·2020-01-22

    Assurance Infusion Recalls Quadmix Injection Vials Due to Sterility Concerns

    Assurance Infusion is recalling 190 vials of Quadmix injection nationwide due to a lack of sterility assurance. The recall covers nine specific lots distributed across the United States.

    Product
    QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0749-2020·2020-01-22

    Assurance Infusion Recalls LIPO B Syringes and Vials for Sterility Concerns

    Assurance Infusion is recalling LIPO B 25MG/50MG/50MG/1000MCG/ML products due to a lack of sterility assurance. The recall covers nationwide distribution.

    Product
    LIPO B 25MG/50MG/50MG/1000MCG/ML (10ML VIAL) in 20 mL syringe and 10 mL vial Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0532-2020·2020-01-22

    Wegmans Signature Crab Cake Recalled for Undeclared Soy

    Wegmans is recalling Signature Crab Cakes because they contain undeclared soy. The products were sold in seven states.

    Product
    Signature Crab Cake; Crab Cake with 2 oz Remoulade Sauce; 1 each; Oven ready tray; various package sizes; Keep Refrigerated
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0546-2020·2020-01-22

    Wegmans Lobster Stuffed Pretzels Recalled for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Pretzels because they contain undeclared soy. The product was sold in seven states.

    Product
    Lobster Stuffed Pretzel; Wegmans Ready to Cook Lobster Pretzel Twist, 1 each; 15 oz; Oven Ready Tray; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0807-2020·2020-01-22

    Siemens ARTIS pheno X-Ray System Recalled for Potential Collision Sensor Blockage

    Siemens is recalling six ARTIS pheno X-ray systems because a collision sensor may falsely activate, permanently blocking system movement.

    Product
    Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0531-2020·2020-01-22

    Wegmans Recalls Signature Crab Cakes Due to Undeclared Soy

    Wegmans is recalling Signature Crab Cakes in several states because they contain undeclared soy. Consumers should not eat the product and should return it to the store.

    Product
    Signature Crab Cake, Signature Crab Cake (2 pk), and Signature Crab Cake (4pk); Wegmans Ready to Cook Signature Crab Cake; Oven ready tray; various sizes, keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0801-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical is recalling BriteBlade Pro laryngoscope blades because internal components may become loose and enter the patient's mouth.

    Product
    BriteBlade Pro Single-Use Fiber Optic Mac 3, CE01120, Do Not Re-use, Rx Only, REF 040-713U, Sterile EO, Qty 10, (01)15055788723001 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords and the glottis by insertion into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0549-2020·2020-01-22

    Wegmans Lobster Stuffed Portabella Recalled for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Portabella mushrooms because they contain undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Lobster Stuffed Portabella; Wegmans Ready to Cook Lobster Portabella Mushroom, Sold by the lb; Unit size varies; Oven ready tray; Package size varies; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0503-2020·2020-01-22

    Stop and Shop Grilled Salmon Meal Recalled for Undeclared Wheat

    Taylor Farms is recalling Stop and Shop Grilled Salmon meals due to undeclared wheat. Consumers with this product should not eat it.

    Product
    Stop and Shop brand Grilled Salmon meal with cooked brown rice, quinoa blend, broccoli florets, cooked white rice, fire roasted edamame, garlic and herb butter, bell pepper, roasted corn and carrots, Net Wt. 12.8 OZ (363g)
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0533-2020·2020-01-22

    Wegmans Recalls Cajun Tilapia Cake Due to Undeclared Soy

    Wegmans is recalling Cajun Tilapia Cake because it contains undeclared soy. The product was sold in New York, Pennsylvania, Maryland, Virginia, New Jersey, Massachusetts, and North Carolina.

    Product
    Cajun Tilapia Cake; Tilapia cake sold by the 1lb; 1 each; Oven ready tray; various package sizes; Keep Refrigerated
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0535-2020·2020-01-22

    Wegmans Crab Dip Recalled for Undeclared Soy Allergen

    Wegmans Food Markets is recalling Crab Dip with Jalapeno Cheddar Cheese because it contains undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Wegmans Crab Dip with Jalapeno Cheddar Cheese; Sold by the lb; Crab Dip with Jalapeno Cheddar Cheese; Size varies; Oven ready tray; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0504-2020·2020-01-22

    Hannaford Grilled Salmon Meal Recalled for Undeclared Wheat

    Taylor Farms is recalling Hannaford brand Grilled Salmon meals because they may contain undeclared wheat. Consumers with this product should not eat it.

    Product
    Hannaford brand Grilled Salmon meal with cooked brown rice, quinoa blend, broccoli florets, cooked white rice, fire roasted edamame, garlic and herb butter, bell pepper, roasted corn and carrots, Net Wt. 12.8 OZ (363g)
    Category
    Food
    Distribution
    4 states