The Recall Desk

State

New Hampshire product recalls

73,584 recalls have nationwide distribution and so reach New Hampshire. 4,477 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,477
Critical
606
Severe
1,045
Most recent
2026-10-21

Of the 4,477 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 1,045 (23%) are Severe.

These figures cover only the 4,477 recalls whose distribution notice names New Hampshire specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

701–725 of 78061

  • SevereCPSC·26749·2026-09-10

    Victgoal Recalls Children's Bike Helmets for Head Injury Risk

    Victgoal is recalling about 40 children's bike helmets because they violate mandatory safety standards, posing a risk of serious injury or death from head injury.

    Product
    Victgoal Children’s Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26754·2026-09-10

    Wantefully Hair Dryer Brushes Recalled for Electrocution and Burn Hazards

    Guang Zhou is recalling Wantefully hair dryer brushes due to risks of electrocution, shock, and burns. Consumers should stop using the products and contact the company for a refund.

    Product
    Wantefully Hair Dryer Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26763·2026-09-10

    Triumph Recalls 2025-2026 TF450 Motorcycles Due to Engine Crash Hazard

    Triumph is recalling 2025 and 2026 TF450 closed-course competition motorcycles because a seized engine rocker arm can cause a crash, posing a risk of serious injury or death.

    Product
    2025 and 2026 Triumph TF450 models Closed Course Competition Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26755·2026-09-10

    Prepared Hero Recalls Fire Spray Canisters Due to Rupture Risk

    Prepared Hero is recalling about 31,000 Hero Fire Spray Canisters because they may deteriorate and rupture during a fire, posing a risk of serious injury or death.

    Product
    Hero Fire Spray Canisters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V584000·2026-09-10

    Chrysler Recalls Jeep Wagoneer Models for Roof Rack Bolt Defect

    Chrysler is recalling specific Jeep Wagoneer and Grand Wagoneer models because improperly tightened roof rack bolts may allow crossbars to detach, creating a road hazard.

    Product
    JEEP — JEEP GRAND WAGONEER, WAGONEER, GRAND WAGONEER L, WAGONEER L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26753·2026-09-10

    SQT Recalls Lontcs Busy Boards Due to Lead Poisoning Risk

    SQT is recalling Lontcs Busy Boards because the zipper contains lead levels exceeding federal standards, posing a risk of lead poisoning to young children.

    Product
    Lontcs Busy Board
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E064000·2026-09-10

    Chrysler Recalls MOPAR Roof Rack Kits Due to Loose Pivot Bolts

    Chrysler is recalling specific MOPAR roof rack kits because improperly tightened pivot bolts may allow crossbars to detach, creating a road hazard.

    Product
    STRUCTURE:BODY:ROOF AND PILLARS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26748·2026-09-10

    Ricky Joy Recalls Sour Crush Candy Bottles Due to Choking Risk

    Ricky Joy is recalling over 2.3 million Sour Crush Rolling Liquid Candy bottles because the rolling ball can detach, posing a choking hazard.

    Product
    Ricky Joy Sour Crush Rolling Liquid Candy Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V585000·2026-09-10

    Forest River Recalls Lone Star Vans Due to Rearview Camera Defect

    Forest River is recalling 2019-2022 Lone Star Vans because cracks in the microprocessor may prevent the rearview camera from displaying properly, increasing crash risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS LONE STAR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26T014000·2026-09-10

    Wheel Pros Recalls 549 Avix TrailTek RT Tires for Incorrect Markings

    Wheel Pros is recalling 549 Avix TrailTek RT tires because the sidewall is incorrectly labeled 'Not for Highway Use,' failing to meet federal safety standards.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0851-2026·2026-09-09

    Optimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials

    Optimal Balance Pharmacy is recalling 53 vials of Glutathione 200 mg/mL due to bacterial endotoxin contamination.

    Product
    Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3086-2026·2026-09-09

    Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk

    Fresenius Medical Care is recalling 18,600 units of 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.

    Product
    5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0819-2026·2026-09-09

    Baxter Recalls Vasopressin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    VASOPRESSIN IN 0.9% SODIUM CHLORIDE — VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN IN 0.9% SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1309-2026·2026-09-09

    Hampton Grocer Lactation Granola Recalled for Salmonella Contamination Risk

    The Hampton Grocer is recalling Small Batch Lactation Granola due to potential Salmonella contamination. Consumers should stop eating the product and return it for a refund.

    Product
    THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3085-2026·2026-09-09

    Fresenius 5008X Blood Tubing Set Recalled for Potential Blood Leak

    Fresenius Medical Care is recalling 5008X HD/HDF Standard Blood Tubing Sets due to a heightened probability of blood leak from the Arterial Alpha Clip connection.

    Product
    5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3061-2026·2026-09-09

    Medline Eye and Cataract Kits Recalled for Potential Sterility Breach

    Medline is recalling 2,080 eye and cataract preop kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3063-2026·2026-09-09

    Medline Blood Draw and Phlebotomy Kits Recalled for Sterility Breach

    Medline is recalling approximately 996,692 blood draw and phlebotomy kits due to potential sterility breaches in the packaging. The defect may expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V576000·2026-09-09

    Ford Recalls 2026 F-150s Due to Rear Axle Bearing Defect

    Ford is recalling 2026 F-150 vehicles because incorrect rear axle tail bearings may cause wheel lock-up or driveshaft separation, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0809-2026·2026-09-09

    Baxter Recalls Famotidine Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Famotidine Injection due to CGMP deviations. The product was distributed in the US, Puerto Rico, and Chile.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0810-2026·2026-09-09

    Baxter Recalls Dexmedetomidine Hydrochloride Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Dexmedetomidine Hydrochloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0821-2026·2026-09-09

    Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Daptomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall covers the US, Puerto Rico, and Chile.

    Product
    Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3084-2026·2026-09-09

    Fresenius Medical Care Recalls 5008X Standard HD Pre-Flush Blood Tubing Sets

    Fresenius Medical Care is recalling 120 units of 5008X Standard HD Pre-Flush Blood Tubing Sets due to a heightened probability of blood leaks during treatment.

    Product
    5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
    Category
    Medical Device
    Distribution
    Distributed nationwide