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.

33926–33950 of 78223

  • ModerateFDA (Devices)·Z-2359-2019·2019-09-04

    Agilent MassHunter Software Recall Due to Sample Data Mismatch

    Agilent Technologies is recalling MassHunter Quantitative Analysis Software versions B.07 or below due to a defect that causes sample name mismatches and prevents saving changes.

    Product
    MassHunter Quantitative Analysis Software, Version B.07.01, used with Triple Quadrupole Mass Spectrometers, models K6460 and K6420 Product Usage: A mass spectrometer for clinical use is a device intended to identify inorganic or organic compounds (e.g., lead, mercury, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2366-2019·2019-09-04

    Bausch & Lomb Recalls Laseredge Knives Due to Possible Dull Edge

    Bausch & Lomb is recalling specific Laseredge Knives used in ophthalmic surgery because they may have dull edges.

    Product
    Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED, REF E7599 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2417-2019·2019-09-04

    Stryker Endotrac Triangle Blade Recall Due to Compromised Sterile Bag Seal

    Stryker GmbH is recalling 1,533 Endotrac EPF/EGR Triangle Blades because the sterile bag seal integrity may be compromised, potentially affecting sterility.

    Product
    Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1846-2019·2019-09-04

    Alkermes Recalls Vivitrol Kits Due to Incorrect Needle Packaging

    Alkermes is recalling 6,514 Vivitrol kits because 1-inch needles were incorrectly placed in sleeves labeled for 1.5-inch needles. The drug vials are not impacted.

    Product
    VIVITROL — VIVITROL (NALTREXONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1839-2019·2019-09-04

    Akorn Recalls Eptifibatide Injection Vials Due to Impurity

    Akorn, Inc. is recalling 4,085 vials of Eptifibatide Injection because they failed impurity specifications for D-aspartic acid.

    Product
    Eptifibatide Injection, 75 mg/100 mL (0.75 mg/mL), 100 mL Single-use Vial, For Intravenous Use Only, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-903-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1841-2019·2019-09-04

    Akorn Recalls Eptifibatide Injection Vials Due to Impurity

    Akorn, Inc. is recalling Eptifibatide Injection vials because they failed impurity specifications for D-aspartic acid.

    Product
    Eptifibatide Injection, a) 20 mg/10 mL (2 mg/mL),10 mL Single Use Vial, NDC 17478-902-10, b) 200 mg/100 mL (2 mg/mL), 100 mL Single-use Vial, NDC 17478-902-90, For Intravenous Use Only, Rx Only, Manufactured by: Akorn Inc., Lake Forest, IL 60045.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1840-2019·2019-09-04

    Akorn Recalls Eptifibatide Injection Vials Due to Fill Volume and Impurity Issues

    Akorn, Inc. is recalling 648 vials of Eptifibatide Injection because the fill volume was below specification and a known impurity exceeded limits.

    Product
    Eptifibatide Injection, 75 mg/100 mL (0.75 mg/mL), 100 mL Single-use Vial, For Intravenous Use Only, Rx Only, Manufactured by: Akorn Inc., Lake Forest, IL 60045, NDC 17478-903-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V640000·2019-08-30

    Lion Recalls 2018 Electric School Buses Due to Brake Connector Issue

    Lion Electric Company is recalling 2018 Lion C electric school buses because loose auxiliary brake pump connectors may cause loss of braking ability if the main pump fails.

    Product
    LION — LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19197·2019-08-30

    RH Recalls Children's Chairs and Stools Due to Lead Paint Violation

    RH is recalling about 3,200 children's chairs and stools sold in the U.S. and Canada because the paint contains lead levels exceeding federal bans.

    Product
    Children's chairs and stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19196·2019-08-30

    RH Recalls Ultra-Soft Turkish Robes for Flammability Standard Violations

    RH is recalling about 5,400 Ultra-Soft Turkish robes because they fail federal flammability standards, posing a burn risk. Consumers should stop using them and request a refund.

    Product
    Ultra-Soft Turkish robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19C001000·2019-08-30

    WAYB Recalls Pico Child Seats Due to Headrest Frame Breakage Risk

    WAYB is recalling Pico child seats manufactured between February and August 2019 because the headrest frame can break and detach, increasing injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19775·2019-08-30

    GreatCall Recalls Lively Mobile Plus Emergency Alert Devices

    GreatCall is recalling Lively Mobile Plus emergency alert devices because the call button may fail during an emergency. No injuries have been reported.

    Product
    Lively Mobile Plus Emergency Alert Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V637000·2019-08-29

    Chrysler Recalls 2019-2020 Jeep Cherokee for Steering Rack Gear Defect

    Chrysler is recalling 2019-2020 Jeep Cherokee vehicles because the steering rack gear may break, potentially causing a loss of steering control and increasing crash risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V632000·2019-08-29

    Ford Recalls 2013-2016 Fusion, MKZ, Edge, and MKX for Steering Defect

    Ford is recalling 116,160 vehicles because road salt may corrode steering bolts, causing loss of power steering assist and increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD MKZ, EDGE, FUSION, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19192·2019-08-29

    Decathlon Recalls Rocky Screwgate Carabiners Due to Unlocking Risk

    Decathlon USA is recalling about 50 Rocky Screwgate carabiners because incorrect assembly can cause them to unlock while in use, posing a risk of serious injury or death.

    Product
    Rocky Screwgate carabiners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19195·2019-08-29

    Pearhead Recalls Ubbi Connecting Bath Toys Due To Choking Hazard

    Pearhead is recalling Ubbi Connecting Bath Toys because they can break and create sharp points, posing choking and laceration hazards to young children.

    Product
    Ubbi Connecting Bath Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V635000·2019-08-29

    2019 Ram 2500 and 3500 Trucks Recalled for Brake Caliper Defect

    FCA US is recalling 2019 Ram 2500 and 3500 trucks because incorrect assembly fluid in brake calipers may cause seals to swell, leading to dragging brakes and increased crash risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19193·2019-08-29

    Rite Aid Recalls Folding Patio Chairs Due to Fall Hazard

    Rite Aid is recalling about 18,800 folding patio chairs because the frames can bend, causing users to fall and potentially get injured.

    Product
    Folding patio chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1843-2019·2019-08-28

    SCA Pharmaceuticals Recalls Ketamine Injection Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 922 syringes of Ketamine 50 mg/5 mL injection due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.
    Category
    Drug
    Distribution
    Distributed nationwide