The Recall Desk

State

Massachusetts product recalls

73,376 recalls have nationwide distribution and so reach Massachusetts. 8,241 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,241
Critical
1,181
Severe
2,353
Most recent
2026-10-07

Of the 8,241 recalls naming Massachusetts we have scored against our rubric, 1,181 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,353 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,241 recalls whose distribution notice names Massachusetts specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18476–18500 of 81617

  • HighFDA (Food)·F-0443-2023·2023-03-22

    NGMO Ballard Semisweet Chocolate Wafer Recalled for Undeclared Peanut Residue

    Clasen Quality Chocolater is recalling NGMO Ballard Semisweet Chocolate Wafer due to possible undeclared peanut residue. Consumers with peanut allergies who may have purchased this product should not consume it.

    Product
    NGMO Ballard Semisweet Chocolate Wafer, Item # 59343. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Chocolate Liquor (Processed with Alkali), Sugar, Cocoa Butter, Butterfat (Milk), Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1256-2023·2023-03-22

    Ambulance cot may separate due to insufficient epoxy in assemblies

    Stryker's Power-PRO 2 ambulance cots may separate at head or foot due to insufficient epoxy. Four affected units in NY and VA should be removed from service immediately.

    Product
    Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2023·2023-03-22

    Bard Mission Disposable Core Biopsy Instrument Kit Recall: Sizing Incompatibility

    Bard Peripheral Vascular is recalling certain Bard Mission Disposable Core Biopsy Instrument Kits due to sizing incompatibility between the biopsy instrument and coaxial needle, which could cause procedural delays or needle breakage.

    Product
    Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1238-2023·2023-03-22

    BD Insulin Syringes Recalled Due to Nonsterile Condition

    BD Insulin Syringes (Catalog 329420) are being recalled due to nonsterile conditions that could expose patients to pathogenic microorganisms and increase infection risk. The recall affects 961,000 units distributed worldwide.

    Product
    BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml, 12.7mm, 28G Single Unit Scale. Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329420
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0610-2023·2023-03-22

    Soybean Lecithin Powder Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling 575 cases of soybean lecithin powder due to undeclared peanut allergen. Affected products were distributed nationwide to manufacturers.

    Product
    Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0607-2023·2023-03-22

    Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling sunflower lecithin powder in 44 lb. boxes due to an undeclared peanut allergen. The affected product poses a serious risk to consumers with peanut allergies.

    Product
    Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1251-2023·2023-03-22

    BioFire BCID2 Diagnostic Panels Recalled for Temperature-Related Performance Issues

    BioFire Diagnostics is recalling BioFire BCID2 diagnostic panels that experienced temperature excursions during shipment, which may reduce their performance. Affected kits were distributed in Florida and Georgia.

    Product
    In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0462-2023·2023-03-22

    Clobazam tablets recalled for potential manufacturing cross-contamination risk

    Breckenridge Pharmaceuticals is recalling certain lots of Clobazam 10 mg tablets due to a potential cross-contamination risk stemming from manufacturing process deviations.

    Product
    Clobazam Tablets, 10 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-900-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0427-2023·2023-03-22

    White Chocolate Wafer Recalled for Undeclared Peanut Residue

    Clasen Quality Chocolate is recalling DF FT Simple Free White Wafer (Item #12935) due to undeclared peanut residue. Consumers with peanut allergies should avoid this product.

    Product
    DF FT Simple Free White Wafer (MB), Item # 12935. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernal Oil, Natural Flavor, Sunflower Lecithin (an emulsifier), and Salt. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive, Madison, WI…
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1252-2023·2023-03-22

    BioFire Respiratory Panel 2.1 Recalled Due to Temperature Shipping Excursions

    BioFire Diagnostics is recalling BioFire Respiratory Panel 2.1 (RP2.1) diagnostic kits due to temperature excursions during shipping that may reduce device performance.

    Product
    In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1) - REF 423742
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2023·2023-03-22

    In Vitro Diagnostic GI Panel Recalled Due to Temperature Exposure During Shipping

    BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.

    Product
    In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - REF RFIT-ASY-0116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0620-2023·2023-03-22

    Egg Roll Wrappers Recalled Due to Undisclosed Peanut Contamination

    Baily International Foods is recalling 1,145 boxes of frozen egg roll wrappers due to peanut contamination in a sub-ingredient. The affected product was distributed to wholesalers in 19 states for restaurant and institutional use.

    Product
    Egg roll wrappers, 6" x 6" and 7" x 7", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.
    Category
    Food
    Distribution
    19 states
  • ModerateFDA (Food)·F-0433-2023·2023-03-22

    DF 85% Cacao Chocolate Wafers Recalled for Undeclared Peanut Residue

    Clasen Quality Chocolate is recalling DF 85% Cacao Bittersweet Chocolate Wafers (Item #54213, Lot #2347T540CL14) because the product may contain undeclared peanut residue, which poses a risk to consumers with peanut allergies.

    Product
    DF 85% Cacao Bittersweet Chocolate Wafer, Item # 54213. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Chocolate, Sugar, Sunflower Lecithin (an emulsifier), and Natural Vanilla Flavor. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive, Madison…
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Food)·F-0609-2023·2023-03-22

    Organic Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling Organic Sunflower Lecithin Powder (44 lb boxes) due to undeclared peanut allergen. The product was distributed to a distributor in Missouri and then nationwide to manufacturers.

    Product
    Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0622-2023·2023-03-22

    Canton Dry Noodle Recalled for Peanut Contamination

    Baily International Foods is recalling Canton Dry Noodle products due to peanut contamination in a sub-ingredient. The affected products were distributed to wholesalers in 19 states for restaurant and institutional use.

    Product
    Canton Dry Noodle, packaged in 30lb. corrugated (cardboard) boxes.
    Category
    Food
    Distribution
    19 states
  • ModerateFDA (Food)·F-0580-2023·2023-03-22

    Two Rivers Coffee pods recalled for undeclared peanut residue

    Two Rivers Coffee hot cocoa pods in variety packs may contain undeclared peanut residue. Consumers with peanut allergies should not consume these products and should check the affected product codes.

    Product
    Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection packaged in single serve pods. Pods are packaged in the following Two Rivers Variety Pack boxes: -Two Rivers Coffee Hot Cocoa Pods, Single Serve Variety Sampler Pack , 40 Count UPC: 810683022554 -Two Rivers Coffee Hot…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0466-2023·2023-03-22

    Buprenorphine Transdermal System 20 mcg/hour Recalled for Specification Failure

    AVEVA Drug Delivery Systems recalls Buprenorphine Transdermal System 20 mcg/hour (Lot 51836) nationwide due to degradation product impurity exceeding specification limits during stability testing.

    Product
    Buprenorphine Transdermal System, CIII 20 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7079-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0464-2023·2023-03-22

    Evamist (Estradiol) Transdermal Spray Recalled for Failed Content Uniformity

    Padagis US LLC is recalling 43,238 cartons of Evamist (Estradiol) transdermal spray nationwide because the spray content uniformity specification for standard deviation was not met at the 18-month stability time point.

    Product
    EVAMIST — EVAMIST (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0430-2023·2023-03-22

    Semisweet Chocolate Drops Recalled for Undeclared Peanut Residue

    Clasen Quality Chocolater recalls 1M Simply Free Semisweet Chocolate Drops due to potential undeclared peanut residue. Consumers with peanut allergies should not consume this product.

    Product
    1M Simply Free Semisweet Chocolate Drop (FT), Item # 53384. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Chocolate Liquor, Cocoa Butter, Sunflower Lecithin (an emulsifier), and Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Drugs)·D-0465-2023·2023-03-22

    Buprenorphine Transdermal System Recalled for Failed Impurity Specifications

    AVEVA Drug Delivery Systems recalls nationwide batches of Buprenorphine Transdermal patches due to a degradation impurity exceeding acceptable limits during stability testing.

    Product
    Buprenorphine Transdermal System, CIII 10 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7077-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E022000·2023-03-20

    Meritor Recalls Front Drive Steer Axles Due to Loose Fasteners

    Meritor is recalling specific front drive steer axles because fasteners may not be tightened sufficiently. This defect could cause axle separation and loss of vehicle control.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V186000·2023-03-20

    Kentucky Trailer XL-12 Recalled for Winch Remote Water Ingress Risk

    Kentucky Trailer is recalling 2021-2022 XL-12 trailers because water in the winch remote can cause corrosion and unintentional operation, increasing injury risk.

    Product
    KENTUCKY TRAILER — KENTUCKY TRAILER XL-12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V183000·2023-03-20

    Prevost Recalls H3-45 Buses for Hazard Light Software Defect

    Prevost is recalling 2022-2023 H3-45 buses because hazard lights may not flash simultaneously when the ignition is off, increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V187000·2023-03-20

    INFINITI QX50 and QX55 vehicles recalled for defective front door lock

    Nissan North America is recalling certain 2022 INFINITI QX50 and 2023 QX55 vehicles due to an incorrect door latch that may prevent the front right-side door from locking automatically, potentially allowing the door to open during a crash.

    Product
    INFINITI — INFINITI QX50, QX55
    Category
    Vehicle
    Distribution
    Distributed nationwide