The Recall Desk

State

New Hampshire product recalls

73,100 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,472
Critical
606
Severe
858
Most recent
2026-09-23

Of the 4,472 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 858 (19%) are Severe.

These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10801–10825 of 77572

  • HighFDA (Devices)·Z-2402-2024·2024-07-24

    Outlook IV Infusion Pump Set Recalled Due to Backcheck Valve Malfunction Risk

    B. Braun is recalling Outlook IV pump sets due to potential backcheck valve malfunction that could allow medication backflow and prevent proper priming, posing a risk of adverse drug reactions and medication loss.

    Product
    Outlook OUTLOOK PUMP SET,3 CARESITE LADS,115 IN. Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490361
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2385-2024·2024-07-24

    B. Braun Infusomat 60 IV Pump Sets Recalled for Backcheck Valve Malfunction

    B. Braun is recalling Infusomat 60 infusion pump sets (Model 363010) due to potential backcheck valve malfunction. The defect could cause medication to flow backward into primary IV containers and prevent proper medication delivery.

    Product
    Infusomat 60 DROP METRISET PUMP SET,3 SFLINE ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2363-2024·2024-07-24

    Abbott Proclaim 7 Pulse Generator Battery Life Shorter Than Labeled

    Abbott is recalling approximately 457 Proclaim 7 Implantable Pulse Generators because the battery may reach end of service sooner than indicated in labeling. Patients may require unexpected device replacement.

    Product
    Abbott Proclaim 7 Implantable Pulse Generator, REF 3667, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2381-2024·2024-07-24

    Infusion pump set backcheck valve malfunction may prevent medication delivery

    B. Braun Medical is recalling an infusion pump set due to potential backcheck valve malfunction that could cause medication to flow backward into IV containers and prevent proper medication administration. The recall affects 3,624 units distributed worldwide.

    Product
    Infusomat UNIV. 15 DROP PUMP SET W/ 0.2 FILTER- Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1509-2024·2024-07-24

    Snapchill Coffee and Oat Milk Beverage Recall Due to Potential Under-Processing

    Snapchill, LLC is recalling 549,146 cans of Coffee + Oat Milk Canned Beverage distributed nationwide and in Canada due to potential under-processing that may not have eliminated harmful organisms.

    Product
    Coffee + Oat Milk Canned Beverage packaged under the following brands and sizes: 1. Dreamy Coffee Co. Hint of Chocolate, 12 oz. 2. Shirazi Distribution Cafe Au Lait - Little Wolf Corree Roasters, 12 oz. UPC 8 50044-13040 5.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2403-2024·2024-07-24

    IV Infusion Pump Set Recalled for Backcheck Valve Malfunction Risk

    B. Braun is recalling the Infusomat UNIV. 15 DROP PUMP SET due to potential backcheck valve malfunction that could cause medication backflow and loss. The defect may result in adverse drug reactions or improper medication delivery.

    Product
    Infusomat UNIV. 15 DROP PUMP SET, 3 ULTRASITE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 363230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2351-2024·2024-07-24

    BD Multitest 6-Color TBNK Reagent Contamination May Cause Erroneous Results

    BD Multitest 6-Color TBNK flow cytometry reagent contains contaminated antibodies that may produce erroneous or delayed test results, potentially impacting clinical decisions.

    Product
    BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF: 337166; BD Multitest 6-Color TBNK, IVD, REF: 662967; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes IVD, REF: 662995. BD Multitest" 6-Color TBNK reagent wit
    Category
    Medical Device
    Distribution
    34 states
  • ModerateNHTSA·24V555000·2024-07-24

    Thomas Built school bus emergency exit labels use lettering too small

    Daimler is recalling certain 2019-2022 Thomas Built school buses because the emergency exit label lettering is too small and may be difficult to read. 27,494 units affected.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, MINOTOUR DRW, SAF-T-LINER C2 JOULEY, MINOTOUR SRW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0610-2024·2024-07-24

    OTC Oral Care Rinse Recalled Due to Microbial Contamination

    StellaLife VEGA Oral Care Peppermint rinse is recalled nationwide due to microbial contamination with Terribacillus species. The affected product was distributed to 60 physician offices.

    Product
    STELLALIFE VEGA ORAL CARE PEPPERMINT — STELLALIFE VEGA ORAL CARE PEPPERMINT (AZADIRACHTA INDICA, CALENDULA, ECHINACEA PURPUREA, PLANTAGO MAJOR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0607-2024·2024-07-24

    Prescription Potassium Chloride Extended-Release Capsules Recalled for Manufacturing Deviations

    Glenmark Pharmaceuticals is recalling Potassium Chloride Extended-Release Capsules nationwide due to manufacturing practice deviations. The voluntary recall affects multiple lot numbers, with no reported illnesses or injuries.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1503-2024·2024-07-24

    Emergency Medical Coffee Sweet Cream Canned Beverage Recalled for Potential Under-Processing

    Snapchill, LLC is recalling Emergency Medical Coffee Sweet Cream canned beverages due to potential under-processing. The recall affects 549,146 cans with expiration dates June 16, 2024–April 16, 2025, distributed nationwide in the US and Canada.

    Product
    Coffee + Non-Dairy Creamer + Sugar-Free Sweetener Canned Beverage packaged under the following brands and sizes: 1. Emergency Medical Coffee Sweet Cream, 12 oz. UPC 8 10149-37035 9.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V550000·2024-07-23

    Indian motorcycle rear suspension pushrods may buckle under load

    Indian Motorcycle is recalling certain 2024 Chieftain, Challenger, Pursuit, Roadmaster and Springfield motorcycles because the rear suspension pushrod may buckle under load.

    Product
    INDIAN — INDIAN ROADMASTER ELITE, SPRINGFIELD, ROADMASTER LIMITED, SPRINGFIELD DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V545000·2024-07-23

    Capacity Recalls 2023 TJ Series Vehicles Due to Steering Gear Defect

    Capacity of Texas is recalling 2023 TJ 5000, 6500, and 9000 vehicles because steering gear assemblies may have fewer recirculating balls than required, risking loss of steering control.

    Product
    CAPACITY — CAPACITY TJ 5000, TJ 9000, TJ 6500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V551000·2024-07-23

    Storyteller Overland Recalls 2024 GXV Next for Incorrect Load Label

    Storyteller Overland is recalling 2024 GXV Next vehicles because incorrect cargo capacity labels may allow overloading, increasing crash risk.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV NEXT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V548000·2024-07-23

    Gulf States Toyota vehicles carry incorrect maximum capacity weight labels

    Gulf States Toyota is recalling a range of Toyota models because the maximum capacity weight value on the label is incorrect. 33,848 units are affected.

    Product
    TOYOTA — TOYOTA LAND CRUISER HYBRID, VENZA HYBRID, TUNDRA HYBRID, TACOMA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V546000·2024-07-22

    Motiv recalls electric chassis vehicles due to high-voltage software defect

    Motiv Power Systems is recalling 2019-2024 electric chassis vehicles because a software error may shut down high-voltage batteries, causing loss of power steering and braking.

    Product
    MOTIV — MOTIV F-53 BEV CHASSIS, F-59 BEV CHASSIS, E-450 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V547000·2024-07-22

    Motiv E-450 BEV Chassis Recalled for Wiring Damage Risk

    Motiv Power Systems is recalling 2021-2024 E-450 BEV chassis vehicles because damaged CAN signal wires could cause a loss of drive power, increasing crash risk.

    Product
    MOTIV — MOTIV E-450 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V543000·2024-07-19

    Blue Bird Recalls School Buses Due to Weak Roof Joints

    Blue Bird is recalling 2019-2023 Vision and All American school buses because roof joints may be too weak, risking panel separation in a crash.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN, ALL AMERICAN SCHOOL BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E061000·2024-07-19

    Ford Recalls Tie Rod Assemblies Due to Potential Steering Failure

    Ford is recalling specific front axle tie rod assemblies because incorrectly heat-treated ball studs may break, potentially causing loss of steering control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V544000·2024-07-19

    Doosan Portable Generator Trailer Recalled for Improperly Tightened Lug Nuts

    Doosan is recalling 2024 Bobcat PG25 portable generator trailers because improperly tightened wheel lug nuts may allow wheels to detach, increasing crash risk.

    Product
    DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V542000·2024-07-19

    Ford Recalls 2023-2024 Transit Vehicles for Steering Assist Loss Risk

    Ford is recalling 2023-2024 Transit vehicles with the Trail package because corrosion in the steering system may cause a loss of power assist, increasing crash risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V538000·2024-07-18

    Chrysler Recalls 2019-2021 Pacifica Plug-In Hybrids for Fire Risk

    Chrysler is recalling 2019-2021 Pacifica Plug-In Hybrids because the battery pack may cause a vehicle fire while parked. Owners should park outside and avoid charging until repairs are completed.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V536000·2024-07-18

    Chrysler Recalls 2017-2018 Pacifica Plug-In Hybrids for Fire Risk

    Chrysler is recalling 2017-2018 Pacifica Plug-In Hybrid vehicles because the battery pack may cause a fire while parked. Owners should park outside and avoid charging until repairs are completed.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24307·2024-07-18

    CFMOTO ZFORCE 950 ROVs Recalled for Crash and Tip-Over Hazards

    CFMOTO is recalling approximately 3,630 ZFORCE 950 HO Sport Side-by-Side recreational off-highway vehicles from 2022–2023 because the shock absorber rod assembly can unthread and detach, causing suspension collapse and crash or tip-over hazards.

    Product
    CFMOTO ZFORCE 950 HO Sport Side-by-Side ROVs (2022-2023)
    Category
    Vehicle
    Distribution
    Distributed nationwide