The Recall Desk

State

New Hampshire product recalls

73,741 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,482
Critical
603
Severe
1,048
Most recent
2026-10-28

Of the 4,482 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,048 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33801–33825 of 78223

  • HighFDA (Food)·F-2124-2019·2019-09-18

    Bubbies Ice Cream Products Recalled for Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and Cookie Dough Ice Cream Bites due to potential foreign plastic pieces.

    Product
    Bubbies Cookie Dough Ice Cream Bites -Sugar Cookie Item Code CDR00004, UPC Code 50014-8, UPC GTIN 10787325500145. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2136-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Red Velvet Item Code CS800180, UPC Code 20086-4, UPC GTIN 10787325200861. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2142-2019·2019-09-18

    Bubbies and Trader Joe's Mochi Ice Cream Recalled for Plastic Pieces

    Bubbies and Trader Joe's are recalling specific mochi ice cream products due to the potential for free-floating foreign plastic pieces.

    Product
    Trader Joes - Vanilla Item Code 64500, UPC Code 00645003. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2130-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Green Tea Item Code CS800056, UPC Code 20023-9, UPC GTIN 10787325200236. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2129-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Chocolate Vanilla Item Code CS812002, UPC Code 20213-4, UPC GTIN 10787325202131. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2137-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Strawberry Item Code CS800014, UPC Code 20073-4, UPC GTIN 10787325200731 Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2133-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Mango Item Code CS800037, UPC Code 20063-5, UPC GTIN 10787325200632. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2122-2019·2019-09-18

    Bubbies Ice Cream Products Recalled for Potential Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and Cookie Dough Ice Cream Bites due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Cookie Dough Ice Cream Bites - Brownie Batter, Item Code CDR00003, UPC 50012-4, UPC GTIN 10787325500121. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2127-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Chocolate Espresso Item Code CS812079, UPC Code 20053-6, UPC GTIN 10787325200533. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2121-2019·2019-09-18

    Martha White Gluten Free Cornbread Mix Recalled for Gluten Presence

    Hometown Food Company is recalling Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix because the product tested positive for gluten despite being labeled gluten-free.

    Product
    Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case. Item UPC: 0 1330082014 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1851-2019·2019-09-18

    Macleods Recalls Pramipexole Dihydrochloride Tablets Due to Subpotency

    Macleods Pharma USA is recalling Pramipexole Dihydrochloride Tablets 0.125 mg because stability studies showed the drug was subpotent.

    Product
    PRAMIPEXOLE DIHYDROCHLORIDE — PRAMIPEXOLE DIHYDROCHLORIDE (PRAMIPEXOLE DIHYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2495-2019·2019-09-18

    Philips 5-Lead ECG Set Recalled Due to Connector Thickness Issue

    Philips is recalling 5-Lead ECG sets because the connector thickness may prevent or impede I 2-Lead ECG measurements.

    Product
    Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Single-Patient-Use ECG lead sets for bedside monitoring are available in 5-lead configuration
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2151-2019·2019-09-18

    FungusAmongUs Shiitake Organic Mushrooms Recalled for Undeclared Sulfites

    Seattle Gourmet Foods Inc. is recalling FungusAmongUs Shiitake Organic Mushrooms due to undeclared sulfites detected by the Florida Department of Agriculture.

    Product
    FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a clear cellophane bag, net Weight 1 ounce. UPC 7 19870 60023 3 for individual 1 ounce bags UPC 50719870600016 for Master caddy that holds 8 packages of 1 ounce bags The label is read in parts…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2488-2019·2019-09-18

    Philips Recalls Two HeartStart MRx Monitor/Defibrillators for Missing Corrections

    Philips North America, LLC is recalling two HeartStart MRx Monitor/Defibrillators because they may not have received applicable corrections from prior field actions.

    Product
    HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx is a lightweight, portable external defibrillator, offering two modes of operation for defibrillation: manual mode and semi-automatic mode (AED). In manual mode, the HeartStart MRx is a full…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2152-2019·2019-09-18

    Stonyfield Kids Strawberry Beet Berry Tubes Recalled for Misbranding

    Stonyfield Farm is recalling 4,064 cartons of Kids Strawberry Beet Berry Tubes because the outer carton labeling does not match the product.

    Product
    Stonyfield Kids Strawberry Beet Berry Tubes, 8 count-2oz each; 453g/package; Keep Refrigerated
    Category
    Food
    Distribution
    6 states
  • LowFDA (Drugs)·D-1848-2019·2019-09-18

    Mylan Recalls Gatifloxacin Ophthalmic Solution Due to Unknown Impurity

    Mylan Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to an out-of-specification result for an unknown impurity.

    Product
    Gatifloxacin Ophthalmic Solution 0.5%, 2.5 mL per bottle, Rx Only, Mfd. for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. Made in India. NDC: 0378-5431-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2490-2019·2019-09-18

    Randox Calibration Serum Recalled for Incorrect Analyte Targets

    Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.

    Product
    This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry assays. Randox calibration sera contain 42 analytes and are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1847-2019·2019-09-18

    Lamivudine Tablets Recalled for Incorrect Package Insert Labeling

    American Health Packaging is recalling Lamivudine Tablets due to an error in the package insert that incorrectly lists tablet description coding.

    Product
    Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V656000·2019-09-17

    McNeilus CNG Trucks Recalled for Pressure Relief Device Defect

    McNeilus is recalling 330 CNG-powered trucks from 2013-2018 because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS MA SIDE LOADER, AUTOREACH, STANDARD MIXER, ZERO RADIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V658000·2019-09-17

    Hyundai Translead Recalls 2017-2018 Duralite HT Flatbed Trailers

    Hyundai Translead is recalling 2017-2018 Duralite HT flatbed trailers because bulkhead brackets may break, causing the bulkhead to detach and create a road hazard.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DURALITE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V659000·2019-09-17

    Terex TLM Aerial Vehicles Recalled for Boom Valve Defect

    Terex is recalling 2016-2017 TLM aerial devices because an incorrect holding valve may cause the boom to drift down if a hose bursts.

    Product
    TEREX — TEREX TLM
    Category
    Vehicle
    Distribution
    Distributed nationwide