The Recall Desk

State

New Hampshire product recalls

73,478 recalls have nationwide distribution and so reach New Hampshire. 4,474 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,474
Critical
606
Severe
1,044
Most recent
2026-10-14

Of the 4,474 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,044 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,474 recalls whose distribution notice names New Hampshire specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22301–22325 of 77952

  • HighFDA (Devices)·Z-0749-2022·2022-03-23

    Abbott Alinity s System software error affects diagnostic analyzer wash cycle

    Abbott Laboratories is recalling 306 units of Alinity s System software version 2.8.0 due to a software error causing insufficient wash buffer volume, which could affect diagnostic test accuracy.

    Product
    Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended for In Vitro diagnostic use only. The Alinity s System is a highthroughput, fully automated immunoassay analyzer designed to determine the presence of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0867-2022·2022-03-23

    Swanson Ultra Vitamin B12 Recalled for Potential Metal Shavings

    Swanson Health Products is recalling Swanson Ultra Vitamin B12 Methylcobalamin supplements due to potential metal shavings in the product. The contamination poses a choking and injury risk.

    Product
    Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per container, Item Code SWU122, UPC 87614-02122. Distributed by Swanson Health Products Fargo, ND 58104. 60 cc green PETE plastic bottle with black 33 induction seal cap
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0764-2022·2022-03-23

    Medical device sterile barrier breach in Boston Scientific HYDRATOME RX

    Boston Scientific is recalling HYDRATOME RX 49-30MM/260CM devices worldwide because sterile barriers are compromised. The manufacturing defect affects device sterility.

    Product
    HYDRATOME RX 49-30MM/260CM Material Number: M00583010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0753-2022·2022-03-23

    Boston Scientific DREAMTOME device recalled due to sterile barrier breach

    Boston Scientific is recalling 12,067 DREAMTOME devices worldwide due to compromised sterility from a sterile barrier breach. The affected units may not be properly protected from contamination.

    Product
    DREAMTOME 44-30MM/260CM Material Number: M00584050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0767-2022·2022-03-23

    Boston Scientific Medical Device Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling 3,330 units of JAGTOME REVOLUTION RX devices due to a sterile barrier breach that compromises device sterility. The devices were distributed worldwide.

    Product
    JAGTOME REVOLUTION RX 39-30-260-025 Material Number: M00584260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0898-2022·2022-03-23

    Taiyaki Variety Pack recalled due to undeclared hazelnut allergen

    FDMR, Inc. (Suji's Korean Cuisine) is recalling Taiyaki Variety Pack because hazelnuts are listed in the ingredient statement but not in the allergen "Contains" statement, posing a risk to consumers with hazelnut allergies.

    Product
    Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container. Item Number 1598329, UPC: 8 50013 07258 3 Three flavors: Chocolate Cream, Vanilla Custard and Red Bean & Cinnamon. Manufactured for Suji's Korean…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2022·2022-03-23

    Sterile barrier breach recalled in Boston Scientific HYDRATOME RX catheters

    Boston Scientific is recalling HYDRATOME RX catheters due to sterile barrier compromise. The 112 affected units worldwide may pose infection risk if used.

    Product
    HYDRATOME RX 49-20MM/260CM Material Number: M00583000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0773-2022·2022-03-23

    Medical Device Sterility Compromise Recall by Boston Scientific

    Boston Scientific has recalled 3,578 units of the JAGTOME RX medical device due to sterility compromise from a barrier breach. Affected units were distributed worldwide.

    Product
    JAGTOME RX 44-20-260-035 Material Number: M00573040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V175000·2022-03-23

    Brake pressure switch corrosion in Arcimoto motorcycles may cause constant brake lights

    Arcimoto Inc. is recalling certain 2019-2022 motorcycles because the brake pressure switch may corrode when exposed to salt and de-icer chemicals. Corroded switches cause brake lights to illuminate constantly, confusing other drivers and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV, RAPID RESPONDER, DELIVERATOR, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0761-2022·2022-03-23

    Boston Scientific Hydratome RX Devices Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling Hydratome RX 44-30MM/260CM devices due to a sterile barrier breach that could compromise device sterility. The recall affects 3,371 units distributed worldwide.

    Product
    HYDRATOME RX 44-30MM/260CM Material Number: M00583050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2022·2022-03-23

    Sterile Barrier Breach in JAGTOME RX Medical Devices Worldwide

    Boston Scientific is recalling 4,487 JAGTOME RX medical devices worldwide due to sterility compromise from a sterile barrier breach. Users face contamination risk if devices are used.

    Product
    JAGTOME RX 39-20-260-025 Material Number: M00573080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0770-2022·2022-03-23

    Boston Scientific JAGTOME RX medical device recalled for sterile barrier breach

    Boston Scientific has recalled 1,447 units of the JAGTOME RX 39-30-260-025 medical device due to a compromised sterile barrier that affects device sterility. The affected devices were distributed worldwide.

    Product
    JAGTOME RX 39-30-260-025 Material Number: M00573100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0758-2022·2022-03-23

    DREAMTOME Medical Device Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling 32 units of DREAMTOME endoscopic devices due to a sterile barrier breach that compromises device sterility, creating potential infection risk. No illnesses have been reported.

    Product
    DREAMTOME 49-30MM/450CM Material Number: M00584030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0860-2022·2022-03-23

    Herbalife Protein Bar Deluxe recalled for undeclared egg allergen

    Herbalife International is recalling Herbalife NutritionProtein Bar Deluxe in Chocolate Peanut flavor nationwide due to undeclared egg allergen. The product poses a risk to consumers with egg allergies.

    Product
    Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars per carton Protein-based snack for energy and nutrition 14 bars 1.23 oz (35 g) each Net wt. 17.3 oz., (490 g) SKU: 0365US Catalog Number: 0365 Formulated and Distributed by Herbalife International of…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0871-2022·2022-03-23

    Honey Sriracha Seasoning Recalled for Undeclared Wheat Allergen

    PS Seasoning & Spices is recalling its Honey Sriracha Snack Stick Seasoning due to undeclared wheat. The product was distributed to multiple U.S. states and Canada.

    Product
    796-B Honey Sriracha Snack Stick Seasoning Net Wt 5.25 lbs. (2.38kg). Part #020001965. Ingredients: Sugar, Salt, Spice, Brown Sugar, Dried Honey, Hot Sauce Powder (aged Cayenne Red Peppers, Vinegar, Salt, Garlic), Garlic Powder, Sodium Diacetate, Sodium Erythorbate…
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0806-2022·2022-03-23

    Syphilis Test Reagent Pack Recalled for Vaccine Interference and Manufacturing Defects

    Bio-Rad's BioPlex 2200 Syphilis Test Reagent Pack is being recalled due to concerns that COVID-19 vaccines may interfere with test results, and due to manufacturing defects affecting reagent stability.

    Product
    BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0800-2022·2022-03-23

    SAFE-T PLUS Adult Lumbar Puncture Tray recalled for manometer failure

    Bard Peripheral Vascular Inc recalled 3,240 SAFE-T PLUS Adult lumbar puncture trays due to manometer failures involving leaking and defective mating connections.

    Product
    SAFE-T PLUS ATRAUMATIC ADULT LP TRAY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0797-2022·2022-03-23

    Lumbar Puncture Tray Devices Recalled for Manometer Leaking and Mating Issues

    Bard Peripheral Vascular Inc. recalls SAFE-T PLUS lumbar puncture trays due to manometer leaking and mating issues affecting device function. The FDA Class II recall covers 15,650 devices distributed nationwide and internationally.

    Product
    SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2022·2022-03-23

    Hologic Panther Fusion Extraction Reagent-X May Produce False Test Results

    Hologic is recalling Panther Fusion Extraction Reagent-X kits due to failed stability specifications that may cause false negative test results. Healthcare providers should stop using affected lots.

    Product
    Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X Fusion Capture reagent-X 4 EA, FER-X Fusion Enhancer Reagent-X (Lithium Hydroxide Solution) 4 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0769-2022·2022-03-23

    JAGTOME RX medical device recalled for sterile barrier breach

    Boston Scientific's JAGTOME RX medical device (367 units) is being recalled worldwide due to a sterile barrier breach that compromises device sterility.

    Product
    JAGTOME RX 39-20-450-025 Material Number: M00573090
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0775-2022·2022-03-23

    Boston Scientific JAGTOME RX device recalled for sterile barrier breach

    Boston Scientific has recalled 2209 units of the JAGTOME RX medical device worldwide due to compromised sterility from a sterile barrier breach. The affected units were distributed across the US and more than 40 countries.

    Product
    JAGTOME RX 44-30-260-035 Material Number: M00573060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0807-2022·2022-03-23

    BioPlex 2200 Syphilis Calibrator Set Recall Due to Vaccine Interference and Reagent Stability Issues

    Bio-Rad Laboratories is recalling 724 BioPlex 2200 Syphilis Calibrator sets due to COVID-19 vaccine interference concerns and manufacturing problems with reagent stability. The recalled lots were distributed nationwide in the U.S. and internationally.

    Product
    BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0869-2022·2022-03-23

    Honey BBQ seasoning recalled due to undeclared wheat allergen

    PS Seasoning & Spices recalls Honey BBQ Snack seasoning (3,001 units) distributed to 28 states and Canada due to undeclared wheat. Consumers with wheat allergies should not use affected lots.

    Product
    Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456. 2. 685-B, Net Wt 5.25 lbs. (2.38kg). Part #020001457. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder…
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0795-2022·2022-03-23

    Lumbar Puncture Tray Adult recalled due to manometer failure and leaking

    Bard Peripheral Vascular Inc is recalling 8,630 lumbar puncture trays due to manometer failure causing leaking and mating issues. Devices were distributed nationwide in the U.S. plus Puerto Rico, Costa Rica, and Hong Kong.

    Product
    LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
    Category
    Medical Device
    Distribution
    Distributed nationwide