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.

36601–36625 of 81989

  • HighFDA (Devices)·Z-2048-2019·2019-07-31

    Cardinal Health Recalls Monoject Blunt Cannulas Due to Sterility Barrier Defect

    Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2040-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect

    Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1523-2019·2019-07-31

    Gericare Iron Supplement Elixir Recalled for Potential Microbial Contamination

    Geritrex, LLC is recalling Gericare Iron Supplement Elixir due to cGMP deviations that may have resulted in microbial contamination.

    Product
    Gericare Iron Supplement Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceuticals Corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-709-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1590-2019·2019-07-31

    Wegmans Carrot Cake Recalled for Potential Plastic Contamination

    Wegmans is recalling Large Ultimate Carrot Cakes because they may contain pieces of plastic. The recall affects 20,232 units sold in six states.

    Product
    Wegmans Large Ultimate Carrot Cake(Carrot Cake with Cream Cheese Frosting), 54oz, Sold in clear plastic cake clam shell, UPC Codes: 77890-82457
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2043-2019·2019-07-31

    Cardinal Health Recalls Monoject 201 Vet Pak Hypodermic Needles

    Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.

    Product
    Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2023-2019·2019-07-31

    Siemens AXIOM Artis dMP X-ray Generator Recall for Power Supply Issue

    Siemens is recalling 32 AXIOM Artis dMP units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.

    Product
    AXIOM Artis dMP, Model Number 7555365
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2029-2019·2019-07-31

    Siemens Artis zee Ceiling Recalled for Power Supply Tolerance Issue

    Siemens Medical Solutions is recalling 428 Artis zee ceiling units due to a power supply tolerance issue that may cause generator failure and prevent X-ray production.

    Product
    Artis zee ceiling, Model Number 10094137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2019-2019·2019-07-31

    Siemens AXIOM Artis dTA X-ray Generator Recall

    Siemens is recalling 178 AXIOM Artis dTA units due to a power supply issue that may prevent X-ray generation during procedures.

    Product
    AXIOM Artis dTA, Model Number 7008605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2028-2019·2019-07-31

    Siemens Artis zee floor recalled for power supply tolerance issue

    Siemens Medical Solutions is recalling 170 Artis zee floor units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.

    Product
    Artis zee floor, Model Number 10094135
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1940-2019·2019-07-31

    Ragu Old World Style Sauce Recalled for Foreign Material

    Mizkan America is recalling 33,864 jars of Ragu Old World Style Sauce due to the presence of foreign material.

    Product
    Ragu Old World Style Sauce Traditional 66oz retail size sold in plastic jar
    Category
    Food
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-2031-2019·2019-07-31

    Siemens Artis zee Biplane Recalled for Generator Power Supply Tolerance Issue

    Siemens is recalling 268 Artis zee biplanes because a power supply tolerance issue may cause generator failure, preventing X-ray production during procedures.

    Product
    Artis zee biplane, Model Number 10094141
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1989-2019·2019-07-31

    Abbott Immunoglobulin G Diagnostic Assay Recall for IFU Updates

    Abbott Laboratories is recalling 11,063 Immunoglobulin G in vitro diagnostic kits to update instructions for use regarding reagents and specimen handling.

    Product
    Immunoglobulin G is an in vitro diagnostic assay for the quantitative determination of immunoglobulin G in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2077-2019·2019-07-31

    Getinge Recalls Seven PulsioFlex Monitoring Systems Due to Error Messages

    Getinge US Sales LLC is recalling seven PulsioFlex Monitoring Systems because they display an internal error message requiring restart or service.

    Product
    PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System is indicated in patients where cardiovascular and circulatory volume status monitoring is necessary. If a patient s biometric data are entered, the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1591-2019·2019-07-31

    Wegmans Ultimate Carrot Cake Slice Recalled for Plastic Contamination

    Wegmans is recalling Ultimate Carrot Cake Slices because they may contain pieces of plastic. Consumers should stop eating the product and return it to the store.

    Product
    Ultimate Carrot Cake Slice (Individual serving slice of Carrot Cake with Cream Cheese Frosting), 6oz, Sold in a clear, square plastic clamshell, UPC Codes: 77890-24956
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2082-2019·2019-07-31

    Medical Intelligence Recalls iGuide System Software Due to False Verification Alerts

    Medical Intelligence Medizintechnik GmbH is recalling iGuide System software versions 2.2.0, 2.2.1, and 2.2.2 because the Constant Correlation Check may incorrectly demand verification scans.

    Product
    IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2014-2019·2019-07-31

    Siemens AXIOM Artis MP X-ray Generator Recall for Power Supply Issue

    Siemens is recalling 24 AXIOM Artis MP units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.

    Product
    AXIOM Artis MP, Model Number 5904466
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1939-2019·2019-07-31

    Ragu Chunky Sauce Recalled for Foreign Material

    Mizkan America is recalling Ragu Chunky Sauce Tomato, Garlic & Onion due to the potential presence of foreign material.

    Product
    Ragu Chunky Sauce Tomato, Garlic & Onion 45oz and 66oz retail sizes sold in plastic jars
    Category
    Food
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1992-2019·2019-07-31

    Abbott C4 In Vitro Diagnostic Assay Recall for Instruction Manual Updates

    Abbott Laboratories is recalling 8,037 C4 in vitro diagnostic assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.

    Product
    C4 is an in vitro diagnostic assay for the quantitative determination of C4 in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light scattering, measured by reading…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1592-2019·2019-07-31

    Wegmans Recalls Carrot Apple Muffins Due to Potential Plastic Contamination

    Wegmans is recalling Carrot Apple Muffins sold in several states because they may contain pieces of plastic.

    Product
    Wegmans Carrot Apple Muffins, Carrot Apple Muffin sold individually on a self-serve bar UPC Codes: 2-08473-00000
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2000-2019·2019-07-31

    Terumo Sur-vet Needle Recall Due to Potential Sterility Compromise

    Terumo Medical Corporation is recalling 638,000 Sur-vet Needles due to a potential loss of package integrity that may compromise sterility.

    Product
    Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-2007-2019·2019-07-31

    Becton Dickinson Recalls 3mL Luer-Lok Syringes With Incorrect Scale Markings

    Becton Dickinson is recalling 3mL Luer-Lok syringes because the scale markings were printed incorrectly, resulting in missing or partially printed numbers and lines.

    Product
    3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-1502-2019·2019-07-31

    Pharma-Natural Recalls Lid O Creme Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling Lid O Creme topical analgesic cream because it was manufactured with current good manufacturing practice violations, including lack of process validation.

    Product
    Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream, 2.5 Oz (71 g) roll on bottle, Manufactured & Distributed by: Pharma Natural, Inc. Hialeah, FL 33016, NDC 63788-111-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1589-2019·2019-07-31

    Wegmans Mini Ultimate Carrot Cake Recalled for Plastic Contamination

    Wegmans is recalling 19,548 units of Mini Ultimate Carrot Cake because the product may contain pieces of plastic.

    Product
    Wegmans Mini Ultimate Carrot Cake (Carrot Cake with Cream Cheese Frosting), 17oz, Sold in clear plastic cake clam shell, UPC Codes: 77890-79304
    Category
    Food
    Distribution
    6 states