The Recall Desk

State

New Hampshire product recalls

72,936 recalls have nationwide distribution and so reach New Hampshire. 4,444 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,444
Critical
596
Severe
846
Most recent
2026-09-09

Of the 4,444 recalls naming New Hampshire we have scored against our rubric, 596 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 846 (19%) are Severe.

These figures cover only the 4,444 recalls whose distribution notice names New Hampshire specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2951–2975 of 77380

  • ModerateFDA (Drugs)·D-0370-2026·2026-03-11

    Med-Nap cleansing towelette bulk packs recalled over manufacturing deviations

    Acme United Corporation is recalling Med-Nap Cleansing Towelettes in bulk cases over current good manufacturing practice deviations.

    Product
    MED NAP CLEANSING TOWELETTE — MED NAP CLEANSING TOWELETTE (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1487-2026·2026-03-11

    Datascope CS300 balloon pump manual recalled for outdated battery specifications

    Datascope is recalling the CS300 IABP running software version C.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.

    Product
    CS300 IABP. Software Version CS300 IABP C.01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0383-2026·2026-03-11

    Midodrine hydrochloride tablets recalled over inadequately sealed blister packaging

    The Harvard Drug Group is recalling one lot of Midodrine Hydrochloride Tablets 5 mg because of a defective container with inadequately sealed blister packaging.

    Product
    MIDODRINE HYDROCHLORIDE — MIDODRINE HYDROCHLORIDE (MIDODRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0364-2026·2026-03-11

    Savannah antibacterial towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Savannah Antibacterial Towelettes over current good manufacturing practice deviations.

    Product
    Savannah Antibacterial Towelettes (Benzalkonium Chloride 0.13%), 1 towelette, 4 x 7, R&R Enterprise, NDC 59647-749-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0372-2026·2026-03-11

    WipesPlus hand sanitizing wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67151-727-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0358-2026·2026-03-11

    First Aid Only BZK antiseptic wipes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY BZK ANTISEPTIC — FIRST AID ONLY BZK ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0368-2026·2026-03-11

    WipesPlus alcohol free BZK wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes over current good manufacturing practice deviations.

    Product
    Wipes Plus, Hand Sanitizing Alcohol Free BZK Wipes (Benzalkonium Chloride 0.13%), Manufactured for: CFS Brands DBA WipesPlus, 4711 E. Heiner Rd. Oklahoma City, OK 73331, NDC 67151-333-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0377-2026·2026-03-11

    Instant hand sanitizing wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Children's Healthcare of Atlanta Instant Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    Children's Healthcare of Atlanta, Instant Hand Sanitizing Wipe(Benzalkonium Chloride 0.13%), 1000 per case, Made in USA for Food Service Resources, Flowery Branch, GA 30542, NDC 0924-7130-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0362-2026·2026-03-11

    Bulk BZK antiseptic towelette brands recalled over manufacturing practice deviations

    Acme United Corporation is recalling BZK Antiseptic Towelettes sold under the Piedmont, Touchpoint, Wellstar Cobb and FSR names over current good manufacturing practice deviations.

    Product
    1) BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) 5"x7" Piedmont Sanitizing Hand Wipes, 1,000 ea Bulk, Made in USA for: Food Service Resources, Flowery Branch, GA 30542, NDC 0924-7130-00. 2) BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) 5" x 7" Touchpoint, 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1492-2026·2026-03-11

    Vascular grafts recalled after expiry dates were calculated from packaging

    Vascutek is recalling Gelsoft Plus and Gelweave vascular prostheses because they were labeled with an additional month of shelf life, expiry having been calculated from packaging rather than gel impregnation.

    Product
    Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE, 631220PE, 631608PE, 631206PE, 631407P50E, 631508PE, 636008PE, 636006PE, 632518PE, 634008PE, 634006PE, 631218PE, 632211PE, 634007PE, 633006PE,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0379-2026·2026-03-11

    Semaglutide compounding ingredient lot recalled over incomplete validation before distribution

    Harbin Jixianglong Biotech is recalling a further lot of Semaglutide for prescription compounding because process validation and bacterial endotoxin method validation were not completed before distribution.

    Product
    Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04 Manufacturer: Harbin Jixianglong Biotech Co., Ltd., North of Baoan Road, East of Changqing Street,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0381-2026·2026-03-11

    Nilotinib capsules recalled after failing appearance tests at six months

    Cipla USA is recalling three lots of Nilotinib Capsules 150 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0382-2026·2026-03-11

    Nilotinib 200 mg capsules recalled after failing appearance tests

    Cipla USA is recalling one lot of Nilotinib Capsules 200 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V135000·2026-03-06

    2026 Kia K4 vehicles recalled for defective rear seat belt anchor

    Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.

    Product
    KIA — KIA K4, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V134000·2026-03-06

    Mercedes-Benz Recalls 2026 GLA 250 for Door Latch Defect

    Mercedes-Benz is recalling 2026 GLA 250 vehicles because an incorrectly installed bowden cable may prevent the door from opening from inside, potentially trapping occupants.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V131000·2026-03-05

    Forest River Recalls 2026 Dynamax Motorhomes Due to Electrical Bonding Defect

    Forest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes because the distribution panel may not be properly bonded to the chassis ground, posing a risk of injury or electrocution.

    Product
    DYNAMAX — DYNAMAX GRAND SPORT GT, EUROPA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V128000·2026-03-05

    Toyota Highlander second-row seat backs may fail to lock

    Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V129000·2026-03-05

    GM heavy duty pickup fuel pump may cause an engine stall

    GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V130000·2026-03-05

    Forest River Recalls 2026 Impression Trailers Due to Wiring Defect

    Forest River is recalling 2026 Impression fifth wheel trailers because exposed wire conductors may cause electrical arcing and increase fire risk.

    Product
    FOREST RIVER — FOREST RIVER IMPRESSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V127000·2026-03-05

    GM Recalls 2025-2026 Chevrolet Express and GMC Savana for Tire Damage

    General Motors is recalling 2025-2026 Chevrolet Express and GMC Savana cutaway vehicles because tires may have sidewall damage, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26317·2026-03-05

    Building block sets recalled because button cell batteries are accessible

    Cubimana Island Storm 3 In 1 Building Sets are being recalled because the battery compartment in the LED light piece lets children access button cell batteries.

    Product
    Cubimana Island Storm 3 In 1 Building Sets with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide