The Recall Desk

State

New Hampshire product recalls

72,913 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.

Which agencies issued them

These figures cover only the 4,444 recalls whose distribution notice names New Hampshire specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1876–1900 of 77357

  • ModerateFDA (Devices)·Z-2150-2026·2026-05-20

    Revolution CT X-ray Computed Tomography System Security Vulnerability Recall

    GE HealthCare is recalling Revolution CT x-ray computed tomography systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription. The vulnerability affects certain Revolution Apex, Revolution Ascend, and Revolution CT systems worldwide.

    Product
    Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0778-2026·2026-05-20

    Swad mango masala candy contains undeclared Blue 1 coloring

    Swad Mango Flavored Masala Candy is being recalled because it contains undeclared Blue 1. The action covers 205 cases.

    Product
    Swad Mango Flavored Masala Candy
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2195-2026·2026-05-20

    Daig Livewire Steerable Electrophysiology Catheter Incomplete Seals Recall

    Stryker Sustainability Solutions is recalling 206 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product. The catheters were distributed nationwide and in Israel and Canada.

    Product
    Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2168-2026·2026-05-20

    Hologic 3DIMENSIONS MAMMOGRAPHY SYSTEM medical device recall

    Hologic is recalling certain 3DIMENSIONS MAMMOGRAPHY SYSTEM models due to internal bolts that may become loose, missing, or broken over time. The FDA classified this as a Class II recall.

    Product
    3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-NS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2170-2026·2026-05-20

    Philips Azurion X-Ray System Cable Hose Carriers May Loosen or Break

    Bolts and plastic parts of cable hose carriers on Philips Azurion X-ray systems may loosen or break during monitor movement or rotation, potentially causing the cable hose to become unsecured.

    Product
    Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230), Azurion 5 (722281), Azurion 5 M12 (722227, 722231), Azurion 5 M20 (722228, 722232, 722281), Azurion 7 (722282), Azurion 7 B12 (722225, 722235), Azurion 7 B20 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2149-2026·2026-05-20

    Revolution Ascend CT scanner security vulnerability affecting AW Server

    GE HealthCare is recalling Revolution Ascend computed tomography systems due to a potential security vulnerability in the AW Server used with Edison Health Link-based CT Smart Subscription. 25 units are affected nationwide.

    Product
    Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2190-2026·2026-05-20

    Reprocessed Electrophysiology Catheter with Incomplete Sterile Seals

    Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging, which may compromise sterility.

    Product
    Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0547-2026·2026-05-20

    Metoprolol Succinate Extended-Release Tablets Recalled Due to Failed Dissolution

    Ascend Laboratories is recalling 17,304 bottles of Metoprolol Succinate Extended-Release 25 mg tablets (Lot #25140859, expiring Jan 2027) distributed nationwide because the tablets failed dissolution specifications, which may affect drug effectiveness.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE ER TABLETS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V314000·2026-05-18

    Hyundai Ioniq rear suspension fasteners may loosen and detach

    Hyundai is recalling certain 2025 Ioniq 5 and 2026 Ioniq 9 vehicles because the rear suspension fasteners may loosen and detach, which can cause a loss of vehicle control.

    Product
    HYUNDAI — HYUNDAI IONIQ 5, IONIQ 9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V313000·2026-05-18

    2026 Keystone Alpine recreational trailers recalled for loose shock bolts

    Keystone RV Company is recalling certain 2024–2026 recreational trailers because shock bolts may have been incorrectly tightened, which could cause loss of vehicle stability and increase crash risk.

    Product
    KEYSTONE — KEYSTONE ALPINE, COUGAR, MONTANA, WALKABOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V316000·2026-05-18

    2025–2026 Hyundai Tucson and Santa Cruz Front Camera Software Issue

    Hyundai is recalling certain 2025 and 2026 Tucson, Tucson Hybrid, Tucson PHEV, and Santa Cruz vehicles due to front camera software that may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI TUCSON, TUCSON PLUG-IN HYBRID, SANTA CRUZ, TUCSON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V315000·2026-05-18

    Tesla 2025-2026 Model Y Vehicles Missing Certification Label

    Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V310000·2026-05-15

    Altec Recalls Aerial Devices Due to Emergency Stop Failure

    Altec is recalling specific aerial device vehicles because the ground-level emergency stop may fail to halt hydraulic functions in ePTO mode, increasing injury risk.

    Product
    ALTEC — ALTEC AT SERIES, TA SERIES AERIAL DEVICE, AN SERIES AERIAL DEVICE, L SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V307000·2026-05-14

    Hyundai Recalls Elantra Vehicles Due to Air Bag Inflator Rupture Risk

    Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of injury from metal fragments.

    Product
    HYUNDAI — HYUNDAI ELANTRA GT, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26483·2026-05-14

    Misco Sports Badminton Toy Sets Recalled Due to Battery Ingestion Risk

    Missry Associates is recalling Misco Sports Badminton Toy Sets because the shuttlecocks contain button cell batteries that children can easily access and swallow, potentially causing serious internal injuries or death.

    Product
    Misco Sports Badminton Toy Sets Red/Blue MT2383
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26490·2026-05-14

    Guidecraft Kitchen Helper Towers Recalled Due to Fall Hazard Risk

    Guidecraft Kitchen Helper Towers are being recalled because the internal platform can loosen, become unstable, or detach, creating a fall hazard for young children. The company has received 11 reports of falls, including three injuries.

    Product
    Guidecraft Kitchen Helper Towers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V304000·2026-05-14

    GMC and Other Full-Size SUVs with Faulty Front Wheel Hub Bolts

    General Motors is recalling certain 2025–2026 GMC Yukon, Yukon XL, Chevrolet Tahoe, Suburban 1500, and Cadillac Escalade models with 24-inch wheels due to incorrectly installed front wheel hub bolts that may loosen or break, risking loss of vehicle control.

    Product
    GMC — GMC, CHEVROLET, CADILLAC YUKON, SUBURBAN 1500, TAHOE, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26485·2026-05-14

    Agio Menlo Woven Patio Swings Recalled Due to Fall Hazard Risk

    World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.

    Product
    Agio Menlo Woven Patio Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26481·2026-05-14

    Tiyol Pull String Teething Toys Recalled for Choking Hazard Risk

    Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.

    Product
    Tiyol Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26479·2026-05-14

    Minka Bardon Series Pendant Light Fixtures Recalled Due to Impact Hazard

    Minka Lighting Group is recalling about 170 Bardon Series Pendant Light Fixtures because the frame can detach from the downrod during installation, posing a risk of serious injury or death. One detachment has been reported with no injuries yet.

    Product
    Minka Bardon Series Pendant Light Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26482·2026-05-14

    Can-Am Outlander Pro and Max Pro All-Terrain Vehicles Speed Limiter Malfunction

    BRP US Inc. recalls about 2,820 Can-Am Outlander Pro and Max Pro ATVs with defective Speed Limiter Mode that can cause unexpected speed and acceleration, posing a risk of serious injury or death from crashes.

    Product
    Can-Am Outlander Pro and Max Pro All-Terrain Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26493·2026-05-14

    Cosyland Children's Tower Stools Recalled for Entrapment and Fall Hazards

    Cosyland Children's Tower Stools can collapse, tip over, or trap a child's torso through front and back openings, posing risks of serious injury and death. The firm is aware of 25 reports of stability issues and falls, with eight injuries including a fractured arm.

    Product
    Cosyland Children's Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide