The Recall Desk

State

New Hampshire product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4326–4350 of 77384

  • ModerateFDA (Drugs)·D-0172-2026·2025-11-26

    Perineal antiseptic recalled over contamination found at the manufacturing facility

    DermaRite Industries is recalling 16,006 units of PeriGiene health care antiseptic because it was made at the same facility where other products were found contaminated.

    Product
    PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0173-2026·2025-11-26

    Petrolatum barrier ointment recalled over contamination found at the manufacturing facility

    DermaRite Industries is recalling 381,619 units of PeriGuard Ointment because it was made at the same facility where other products and lots were found to be contaminated.

    Product
    PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0174-2026·2025-11-26

    Zinc oxide barrier cream recalled over contamination found at the facility

    DermaRite Industries is recalling 37,272 tubes of Renew PeriProtect because it was made at the same facility where other products and lots were found to be contaminated.

    Product
    Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0553-2026·2025-11-26

    Sodium fluoride microtubes recalled over an inadequate quality system

    ASP Global is recalling 2,100 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with sodium fluoride, over an inadequate quality system.

    Product
    SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Sodium Fluoride; Gray Model/Catalog Number: 07 7340 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0561-2026·2025-11-26

    Larger sodium heparin capillary tubes recalled over unvalidated manufacturing processes

    ASP Global is recalling 947,100 SAFE-T-FILL plastic blood gas capillary tubes, 150 microlitres with sodium heparin, over an inadequate quality system.

    Product
    SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0007 Product Description: A clear, plastic capillary blood collection tube
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0548-2026·2025-11-26

    Three hundred microlitre clot activator tubes recalled over quality system findings

    ASP Global is recalling 6,600 SAFE-T-FILL micro capillary blood collection tubes, 300 microlitres with clot activator, over an inadequate quality system.

    Product
    SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Clot Activator; Red Model/Catalog Number: 07 7151 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0554-2026·2025-11-26

    Amber clot activator microtubes recalled over an inadequate quality system

    ASP Global is recalling 1,500 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with clot activator in an amber microtube, over an inadequate quality system.

    Product
    SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator; Amber Microtube, Red Model/Catalog Number: 07 7450 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0538-2026·2025-11-26

    Fecal occult blood controls recalled over a wrong expiration date printed

    Polymedco is recalling 403 units of OC-Auto FOBT-CHEK Negative Controls because the kit box and vial labels state an expiration date of 2026-01-16 instead of 2027-01-17.

    Product
    OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult Blood Test)
    Category
    Medical Device
    Distribution
    47 states
  • SevereNHTSA·25V816000·2025-11-25

    Rivian delivery van driver seat belt pretensioner cable can be damaged

    Rivian is recalling certain 2022-2025 EDV vehicles because the driver's seat belt pretensioner cable may become damaged and fail to restrain the occupant as intended in a crash.

    Product
    RIVIAN — RIVIAN EDV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V817000·2025-11-25

    International truck control units can lose ABS and stability control

    International is recalling certain 2016-2026 trucks with Bendix control units because electrical noise may cause the ECU to misprocess commands or stop working, disabling ABS and stability control.

    Product
    INTERNATIONAL — INTERNATIONAL 7600, RH, MV, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V818000·2025-11-25

    Volvo Recalls XC60 Models Due to Improperly Tightened Front Seat Bolts

    Volvo is recalling 2018, 2025, and 2026 XC60 vehicles because front seat bolts may be loose. This defect could prevent seats from restraining occupants during a crash.

    Product
    VOLVO — VOLVO XC60MHEV, XC60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V819000·2025-11-25

    2026 Cadillac Vistiq Electric Vehicles Missing Owner's Manual

    General Motors is recalling certain 2026 Cadillac Vistiq electric vehicles because the radio may not have been configured to download the electronic owner's manual during production. Without access to the manual, owners may not know how to safely use and operate the vehicle.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V815000·2025-11-25

    2026 Chevrolet Silverado 1500, 2500, 3500 Missing Owner Manuals

    General Motors is recalling certain 2026 Chevrolet Silverado 1500, 2500, and 3500 vehicles because some may not have received an owner's manual during production. Without the manual, owners may not know how to safely use child restraint anchorages, increasing crash injury risk.

    Product
    CHEVROLET — CHEVROLET SILVERADO 1500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V812000·2025-11-24

    Newell Recalls 2022 P50 Coaches Due to Seat Mounting Defect

    Newell Coach Corp. is recalling 2022 P50 coaches because improperly welded pedestal mounting plates may cause seat assemblies to detach, increasing crash injury risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V813000·2025-11-24

    Foretravel Recalls Realm and Realm 450 Vehicles for Seat Weld Defect

    Foretravel is recalling 2020-2022 Realm and 2022 Realm 450 vehicles because a seat mounting plate may be improperly welded, allowing the seat to detach.

    Product
    FORETRAVEL — FORETRAVEL REALM, REALM 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V814000·2025-11-24

    nuCamp Trailers Recalled for Incorrect Weight Labels

    Pleasant Valley is recalling 2025-2026 nuCamp trailers because incorrect weight information on labels may lead to unintentional overloading and increased crash risk.

    Product
    NUCAMP — NUCAMP TAG, TAB 400, TAB 360, TAB 320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V810000·2025-11-21

    Altec Recalls 2019-2024 AT Series Vehicles Due to Emergency Stop Defect

    Altec is recalling 2019-2024 AT Series vehicles because the lower emergency stop may not function when the upper control is selected, increasing the risk of death or serious injury.

    Product
    ALTEC — ALTEC AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V806000·2025-11-20

    International trucks may stay in gear with the parking brake applied

    International is recalling certain 2023-2026 LT and RH vehicles because the auto neutral function may not recognise that the parking brake has been applied, leaving the transmission in gear.

    Product
    INTERNATIONAL — INTERNATIONAL RH, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V805000·2025-11-20

    Cemen Tech Recalls Volumetric Mixer Trucks Due to Separation Risk

    Cemen Tech is recalling specific volumetric mixer trucks because mounting plates may crack, allowing the mixer to separate from the vehicle and create a road hazard.

    Product
    CEMEN TECH — CEMEN TECH C60T VOLUMETRIC MIXER, C60 VOLUMETRIC MIXER, M60 VOLUMETRIC MIXER, C60E VOLUMETRIC MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26096·2025-11-20

    Folding learning towers recalled after 14 reports of the platform collapsing

    About 9,780 Grow 'N Stow Folding Learning Towers are being recalled because the platform inside the tower can collapse; 14 collapses have been reported including one child with bruises.

    Product
    Grow 'N Stow Folding Learning Tower
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26103·2025-11-20

    Riding lawn mowers recalled after 15 reports of unexpected bouncing

    About 650 model year 2025 Spartan SRT-XD and KGZ-XD riding mowers are being recalled because incorrectly installed steering arm dampers can cause bouncing and loss of control.

    Product
    Model Year 2025 Spartan SRT-XD and KGZ-XD riding lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide