The Recall Desk

State

New Hampshire product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7551–7575 of 77428

  • SevereNHTSA·25V150000·2025-03-07

    Mercedes-Benz Recalls 2023 EQE Models for Detaching Wheel Rim Inserts

    Mercedes-Benz is recalling 2023 EQE 350 4MATIC and EQE 350+ vehicles because wheel rim inserts may detach while driving, creating a crash hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQE 350+, redundant EQE 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V149000·2025-03-07

    2025 Forest River Aurora Travel Trailers Electrical Fire Risk Recall

    Forest River is recalling certain 2025 Aurora ART26BHS travel trailers because the air conditioner electrical connector may have exposed wiring strands that can cause electrical arcing and fire.

    Product
    FOREST RIVER — FOREST RIVER AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25160·2025-03-06

    Nuby Stroller Fans recalled due to laceration injury hazard

    Nuby Stroller Fans are recalled because the housing allows children's fingers to contact the spinning blade, causing lacerations; six injuries have been reported. Consumers should stop using the product immediately and contact the manufacturer for a free replacement.

    Product
    Nuby Stroller Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25168·2025-03-06

    Children's Nightgowns and Robes Recalled for Flammability and Burn Hazard

    Marie-Chantal children's nightgowns, pajama sets and robes violate federal flammability standards for sleepwear, posing a risk of serious burn injuries. About 560 units sold nationwide from November 2021 through October 2024; consumers should stop use immediately.

    Product
    Marie-Chantal Children's Nightgowns, Pajama Sets and Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25170·2025-03-06

    Auto World Unassembled Slot Cars Recalled for Loose Magnet Ingestion Hazard

    About 55,000 Auto World Unassembled Deluxe Pit Kit Slot Cars are being recalled because loose magnets in unassembled kits pose an ingestion hazard to children. The products were sold nationwide from July 2023 to February 2024.

    Product
    Auto World Unassembled Deluxe Pit Kit Slot Cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25172·2025-03-06

    Love Our Home Crib Bumpers Recalled for Federal Ban Violation and Suffocation Risk

    Love Our Home braided crib bumpers sold on Shein.com violate the federal Safe Sleep for Babies Act and pose a suffocation hazard to infants. About 750 units were sold between March and November 2024.

    Product
    Love Our Home Braided Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V145000·2025-03-06

    Jayco Recalls 2024-2025 Motorhomes Due to Incorrect Federal Load Labels

    Jayco is recalling specific 2024 and 2025 motorhomes because incorrect Federal labels may allow the vehicles to be overloaded, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, ALANTE SE, REDHAWK SE, ODYSSEY SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V147000·2025-03-06

    2024 INEOS GRENADIER door latch assembly defect recall

    INEOS is recalling certain 2024 Grenadier vehicles because the door button mechanism may lack sufficient grease, preventing the door from fully latching. An unlatched door can open unexpectedly while driving, increasing injury risk.

    Product
    INEOS — INEOS GRENADIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V148000·2025-03-06

    Cadillac CT5 and related vehicles transmission lock-up recall

    General Motors is recalling certain 2019–2022 Cadillac and Chevrolet vehicles with 10-speed transmissions due to internal transmission damage that may cause wheel lock-up while driving.

    Product
    CADILLAC — CADILLAC, CHEVROLET CT4, CT6, CT5, CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V146000·2025-03-06

    2024 Kawasaki Z500 and Ninja 500 Motorcycles Clutch Release Shaft

    Kawasaki is recalling certain 2024 Z500 and Ninja 500 motorcycles due to improper welding of the clutch release shaft, which can cause the clutch lever to break and disable the motorcycle, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI Z500, NINJA 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25173·2025-03-06

    Taylor Water Technologies Recalls Phosphate Reagent Bottles Due to Chemical Burn Risk

    Taylor Water Technologies is recalling about 10,000 Phosphate Reagent #1 bottles sold with test kits. The sulfuric acid bottles lack required child-resistant packaging, posing a risk of severe chemical burns.

    Product
    Phosphate Reagent #1 Bottles sold within the Taylor Phosphate Test Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25167·2025-03-06

    BD Recon LT Avalanche Transceivers Recalled Due to Switch Corrosion

    BD Recon LT avalanche transceivers are recalled because the switch mechanism can corrode and fail, potentially preventing rescuers from locating avalanche victims. Six devices have malfunctioned; no injuries reported.

    Product
    BD Recon LT Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0578-2025·2025-03-05

    Gerber Baby Teething Sticks Recalled Due to Choking Risk

    Nestlé-USA is recalling all lots of Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Strawberry Apple flavor following complaints of infant choking. The product was distributed across 42 states and Puerto Rico.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    46 states
  • SevereNHTSA·25V143000·2025-03-05

    Airstream Recalls Classic Travel Trailers Due to Fire Risk

    Airstream is recalling certain Classic travel trailers because the sofa footrest switch wiring may overheat, increasing the risk of a fire.

    Product
    AIRSTREAM — AIRSTREAM CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0579-2025·2025-03-05

    Gerber Baby Soothe 'n' Chew Teething Sticks Recalled for Choking Risk

    Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Banana flavor are recalled nationwide due to complaints of infant choking. All lots in both 1.59 oz and 3.2 oz packages are affected.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    46 states
  • HighFDA (Devices)·Z-1240-2025·2025-03-05

    MRI System May Resume Scanning Above Safe Thermal Limits

    GE Healthcare's Brivo MR355 MRI system can incorrectly resume scans when tissue heating limits are exceeded, potentially causing thermal burns if patients contact conductive materials. The recall affects 22 systems distributed nationwide and internationally.

    Product
    Brivo MR355, NMRI system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1236-2025·2025-03-05

    Video Colonoscope May Cause Thermal Burns to Tissue During Use

    The PENTAX Medical Video Colonoscope (Model EC38-i20cL) can develop excessive heat at the tip during procedures, potentially causing thermal burns to patient tissue. Users reported dark images and steam-like smoke from the device.

    Product
    PENTAX Medical Video Colonoscope- Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastrointestinal tract Model: EC38-i20cL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1215-2025·2025-03-05

    Anatomic Lateral Fibula Plate locking screw malfunction during surgery

    Tyber Medical is recalling 220 A.L.P.S. mvX Anatomic Lateral Fibula Plates due to complaints that the locking screw passes through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770708101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1224-2025·2025-03-05

    A.L.P.S. mvX Medial Tibia Plate Locking Screw Malfunction Recall

    Tyber Medical recalls 208 units of A.L.P.S. mvX Medial Tibia Plates due to locking screws that can pass through the locking hole during surgery, causing surgical delays. No patient injuries have been reported.

    Product
    A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate, 12-Hole, Right Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715122
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1213-2025·2025-03-05

    Orthopedic plate recall: locking screw may pass through hole during surgery

    Tyber Medical is recalling 214 units of A.L.P.S. mvX orthopedic plates (nationwide) because the locking screw may pass through the locking hole during surgery. Surgical delays have been reported.

    Product
    A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended to bridge or otherwise stabilize bone fragments to facilitate healing. Model/Catalog Number: 770708081
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1242-2025·2025-03-05

    MRI Systems May Resume Scans When SAR Exceeds Safe Limits

    Certain GE Healthcare MRI systems may incorrectly enable scan resumption when radiofrequency energy absorption exceeds FDA-set limits, potentially causing tissue heating. Risk is higher for patients with implants or touching conductive materials.

    Product
    SIGNA MR355, SIGNA MR360, NMRI system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V144000·2025-03-05

    Mercedes-Benz Tourrider Buses Recalled for Missing Driver Seat Bracket

    Daimler Coaches is recalling 2022-2025 Mercedes-Benz Tourrider buses because a missing driver's seat bracket may allow the backrest to fold forward in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ TOURRIDER PREMIUM, TOURRIDER BUSINESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2025·2025-03-05

    BD Pyxis Medication Dispensing Devices Labeling Update Addresses Manual Access Risk

    FDA is requiring labeling updates for BD Pyxis automated medication dispensing devices to address the risk of delays in medication access due to power loss or device malfunctions. The recall affects approximately 1,521 units distributed nationwide.

    Product
    BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis user/software/safety guides and quick reference guides.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0580-2025·2025-03-05

    Chocolate Caramels recalled for contamination with plastic pieces

    V Chocolates, Inc is recalling Assorted Chocolate Caramels with kosher sea salt due to plastic pieces from a broken tray. Consumers should not consume this product and should dispose of or return it.

    Product
    Assorted Chocolate Caramels with kosher sea salt, Net Weight 1.25lb
    Category
    Food
    Distribution
    Distributed nationwide