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.

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.

2026–2050 of 77357

  • SevereCPSC·26475·2026-05-07

    Analemma Water Bottles recalled for laceration and ingestion hazards

    Analemma Water Bottles are recalled because the inner glass liner can break, posing risk of serious injury or death from laceration and ingestion. The importer has received 20 reports of the glass breaking, including one oral injury.

    Product
    Analemma Water Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V291000·2026-05-07

    Fontaine Recalls 2025-2026 Fusion Flatbed Trailers Due to Cracked Beams

    Fontaine Trailer Company is recalling 2025-2026 Fusion flatbed trailers because hydrogen contamination during galvanization may cause main beams to crack, risking load loss and crashes.

    Product
    FONTAINE — FONTAINE FUSION FLAT BED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V290000·2026-05-07

    Jeep Cherokee power transfer unit may fail and cause rollaway

    Chrysler is recalling certain 2019-2023 Jeep Cherokee vehicles because the power transfer unit may fail, which can cause a loss of drive power or vehicle rollaway.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26470·2026-05-07

    Multi-Purpose Helmets Recalled for Serious Head Injury Risk

    Multi-purpose helmets sold on Temu by Foubeaka and Geniuss are recalled because they violate mandatory bicycle helmet safety standards and can fail to protect users in a crash, posing a serious risk of injury or death.

    Product
    Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26472·2026-05-07

    Justforjoyful Rainbow Wall Toys Recalled for Choking Hazard Risk

    The CPSC has recalled Justforjoyful Rainbow Wall Toys because the drumstick attached to the xylophone component has a spherical end that violates the mandatory children's toy safety standard and poses a choking hazard. About 160 units were sold on Amazon from December 2025 through March 2026.

    Product
    Justforjoyful Rainbow Wall Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26466·2026-05-07

    Battery-operated Light Up Toys Recalled for Risk of Battery Ingestion

    ZMC Group is recalling about 124,560 battery-operated light-up toys because they contain easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children. Consumers should stop using the toys immediately and contact the manufacturer for a refund.

    Product
    Various Battery-operated Light Up Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26478·2026-05-07

    EVLWZL and Gunugu Mattresses Recalled for Fire Hazard Risk

    EVLWZL and Gunugu mattresses violate mandatory flammability standards and pose a risk of serious injury or death from fire. Approximately 670 units sold through Amazon, Walmart, and Wayfair from October 2025 through March 2026 are affected.

    Product
    EVLWZL and Gunugu Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V289000·2026-05-07

    GMC Yukon and Other GM Vehicles with Transfer Case Defect

    General Motors is recalling certain 2026 GMC Yukon, Sierra 1500, Yukon XL and other GM vehicles, as well as select 2015–2020 models, due to a missing component in the drivetrain transfer case that may cause wheel lockup without warning. The defect increases the risk of a crash.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SILVERADO 1500, SUBURBAN 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26469·2026-05-07

    Rublev Colours Gum Turpentine and Mineral Spirits Bottles Recalled

    Natural Pigments is recalling about 860 bottles of Rublev Colours Gum Turpentine and Mineral Spirits due to non-compliant packaging that poses a risk of serious injury or death from child poisoning.

    Product
    Rublev Colours Gum Turpentine and Mineral Spirits Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26467·2026-05-07

    Favoto Model H-1 Bicycle Helmets Recalled for Serious Head Injury Risk

    Favoto Model H-1 bike helmets violate mandatory safety standards and may fail to protect users in a crash, posing a risk of serious head injury or death. About 2,200 units sold on Amazon from April 2022 through January 2026 are affected.

    Product
    Favoto Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V287000·2026-05-06

    Micro Bird Recalls School Buses Due to Oil Line Fire Risk

    Micro Bird is recalling 2023-2026 G5 and 2024 MB II school buses because a drive belt pulley may damage oil lines, increasing the risk of a fire.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0499-2026·2026-05-06

    Optase Dry Eye Drops Recalled for Lack of Sterility Assurance

    Scope Health is recalling Optase Dry Eye Intense Drops (Glycerin 0.2%) due to lack of assurance of sterility. The product is distributed nationwide.

    Product
    OPTASE — OPTASE (GLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1996-2026·2026-05-06

    iLet Bionic Pancreas Software Versions Recalled for Delayed CGM Readings

    Beta Bionics is recalling iLet Bionic Pancreas units with software versions 1.4.2 and 1.4.3 due to a compatibility issue with Dexcom G7 sensors that can cause delayed glucose readings and loss of automatic insulin adjustments.

    Product
    iLet Bionic Pancreas, REF: BB1001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0491-2026·2026-05-06

    Systane Lubricant Eye Gel Recalled Due to Sterility Concerns

    Alcon Research LLC is recalling Systane Lubricant Eye Gel Night Gel (10g) distributed nationwide due to FDA inspection observations regarding lack of assurance of sterility that may impact product quality.

    Product
    SYSTANE — SYSTANE (HYPROMELLOSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0492-2026·2026-05-06

    GenTeal Tears Lubricant Eye Gel Recalled Due to Sterility Concerns

    Alcon Research LLC is recalling GenTeal Tears Lubricant Eye Gel nationwide due to FDA inspection observations indicating the product may lack assurance of sterility. Consumers should not use affected lots.

    Product
    GENTEAL TEARS — GENTEAL TEARS (HYPROMELLOSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1984-2026·2026-05-06

    Immy Myco DDR Trident Neutralization Buffer B Recalled for Potential Contamination

    Immuno-Mycologics, Inc. is recalling Immy Myco DDR Trident Bulk Neutralization Buffer B (60 X 30 mL, Lot F5061154) because the product may contain contaminants. The buffer is used for clinical specimen processing for Mycobacterium spp. diagnosis.

    Product
    Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V286000·2026-05-06

    Micro Bird Recalls G5 Transit Buses Due to Oil Line Fire Risk

    Micro Bird is recalling 2023-2025 G5 transit buses because a drive belt pulley may damage oil lines, creating a fire risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1992-2026·2026-05-06

    Depuy Synthes ATTUNE Revision Hinge Femoral implants recalled for sterility risk

    DePuy Synthes is recalling ATTUNE Revision Hinge Femoral knee implants because external sterile packaging was found adhered to internal packaging, potentially compromising sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2045-2026·2026-05-06

    Medline medical convenience kits recalled for non-sterile alcohol prep pads

    Medline Industries is recalling multiple medical convenience kits nationwide due to Webcol Large Alcohol Prep Pads that were found to be non-sterile. A contaminant (Paenibacillus phoenicis) was discovered during a routine sterilization dose audit.

    Product
    Medline and Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. LVAD DRIVELINE KIT (Centurion), Medline Kit SKU DT17360 (Centurion); 2. LONG TERM/INPATIENT IV SECUREMENT SET (Centurion), Medline Kit SKU IVS1975A; 3. CVC DRESSING C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2042-2026·2026-05-06

    Medline Centurion Medical Convenience Kits Recalled for Non-Sterility

    Medline Industries is recalling Centurion medical convenience kits containing Webcol Large Alcohol Prep Pads due to discovery of non-sterile product contaminated with Paenibacillus phoenicis bacteria during sterilization testing.

    Product
    Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL PURPOSE TRAY, Medline Kit SKU 75670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1960-2026·2026-05-06

    Philips Ingenia Ambition S MRI Systems Recalled for Stiffness Value Errors

    Philips is recalling certain Ingenia Ambition S MRI systems with MR Elastography software due to potential stiffness value errors that may occur when specific image reconstruction parameters are used in combination with Resoundant's algorithm.

    Product
    Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Model Number (REF): 782108. 3. Model Number (REF): 782139.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1999-2026·2026-05-06

    Abbott i-STAT EG7+ Blood Gas Cartridges Reporting Inaccurate Results

    Abbott Point Of Care is recalling approximately 7.6% of specific i-STAT EG7+ cartridge lots due to a manufacturing issue causing falsely high pCO2 and low pH readings. Inaccurate results could lead clinicians to make unnecessary or harmful medical interventions.

    Product
    i-STAT EG7+ cartridge; List Number: 03P76-25;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1987-2026·2026-05-06

    DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall

    DePuy Synthes is recalling one lot of ATTUNE Revision Hinge Femoral components (left size 7, part number 150450107) due to external sterile packaging adhered to internal packaging, potentially compromising product sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1991-2026·2026-05-06

    Depuy Synthes ATTUNE Revision Hinge Femoral Knee Component Recall

    Depuy Synthes is recalling 3 units of the ATTUNE Revision Hinge Femoral (Right, Size 5, Cemented) knee implant due to external sterile packaging adhered to internal sterile packaging, potentially compromising product sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2026·2026-05-06

    DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall

    DePuy Synthes is recalling 3 units of the ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM due to external sterile packaging found adhered to internal packaging, potentially compromising sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.
    Category
    Medical Device
    Distribution
    Distributed nationwide