State

New Hampshire product recalls

73,096 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,472
Critical: 606
Severe: 858
Most recent: 2026-09-23

Of the 4,472 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 858 (19%) are Severe.

Which agencies issued them

These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10201–10225 of 77568

ModerateFDA (Devices)·Z-2906-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M syringes recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-Millennium Medical (Sol-M) syringes, affecting 126 units distributed nationwide. The recall was initiated following a manufacturer recall of the syringe components.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001712;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2857-2024·2024-09-04
Sol-M Syringes in BVI CustomEyes Procedure Packs Recalled Voluntarily
BVI is recalling CustomEyes Procedure Packs containing syringes from Sol-Millennium Medical due to Sol-M's voluntary recall of those syringes.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001314;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2888-2024·2024-09-04
Syringe Recall: BVI CustomEyes Procedure Packs Distributed Nationwide
Beaver Visitec International voluntarily recalls BVI CustomEyes Procedure Packs containing Sol-M syringes. The affected packs, which contain low dead space and luer slip 1ml syringes, were distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001605;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2918-2024·2024-09-04
CustomEyes Procedure Packs with Sol-M Syringes Recalled by Beaver Visitec International
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs (Lot 6066752) containing Sol-M syringes. Approximately 22 units distributed nationwide in the US have been affected.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001836;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V649000·2024-09-03
2025 Mazda CX-50 Forward Sensing Camera Malfunction Disables Safety Systems
Mazda is recalling 2025 CX-50 and certain 2024 models due to a forward sensing camera malfunction that may prevent automatic emergency braking and lane-keep assist systems from functioning, increasing crash risk.
Product
MAZDA — MAZDA MAZDA3, CX-30, CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V648000·2024-09-03
2023 Nova Bus LFS Buses Recalled for Defective Instrument Panel Firmware
Nova Bus is recalling certain 2023-2024 LFS buses due to defective instrument panel firmware that may fail to display the speedometer or warning lights, and may cause loss of drive power, increasing crash risk.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V646000·2024-08-30
E-One Recalls Cyclone and Typhoon Vehicles Due to Crossmember Defect
E-One is recalling 2022-2024 Cyclone and Typhoon vehicles because a broken engine crossmember can damage the cooling fan, potentially causing an engine stall and increasing crash risk.
Product
E-ONE — E-ONE CYCLONE II, CYCLONE N, TYPHOON N
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E074000·2024-08-30
Alltrade Recalls Kilimanjaro E-bike Racks Due to Connection Point Cracking
Alltrade Tools LLC is recalling Kilimanjaro E-bike racks sold at Costco because connection points may crack, causing the rack to fail and the bicycle to detach.
Product
EQUIPMENT:MECHANICAL:CARRIER/RACK recall
Category
Consumer Product
Distribution
Distributed nationwide
CriticalCPSC·24350·2024-08-29
HALO 1000 Portable Power Stations Recalled for Fire and Burn Hazards
About 5,740 HALO 1000 Portable Power Stations are recalled because their lithium-ion batteries can overheat and catch fire. One death from smoke inhalation and four fire incidents have been reported.
Product
HALO 1000 Portable Power Stations
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24352·2024-08-29
Glow in Dark Party Supplies Toy Sets Recalled for Battery Ingestion Hazard
Glow in Dark Party Supplies Toy Sets sold on Amazon contain button cell batteries in Bunny Ears Headbands that can be easily accessed by children, posing a serious ingestion hazard. The sets violate federal battery-operated toy regulations.
Product
Glow in Dark Party Supplies Toy Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V644000·2024-08-29
Altec Recalls 2024 Spray Trucks and Aerial Devices for Line Security Defect
Altec is recalling 623 units of 2024 spray trucks and aerial devices because fuel or brake lines may not be properly secured, posing risks of brake failure or fire.
Product
ALTEC — ALTEC SPRAY TRUCK, TA CLASS, AT SERIES
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24351·2024-08-29
Fisher-Price Dumbbell Toy Recalled for Choking Hazard
Fisher-Price is recalling a plastic dumbbell toy sold in the Baby Biceps Gift Set because the gray caps on the ends can come off, posing a choking hazard to infants. The firm has received seven reports of the ends coming off but no injuries have been reported.
Product
Dumbbell toy sold with Baby Biceps Gift Set
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2636-2024·2024-08-28
McGrath Mac Video Laryngoscope battery depletion may cause thermal event and explosion
McGrath Mac Video Laryngoscope devices may experience battery management system failures causing batteries to deplete below design thresholds, potentially resulting in thermal events and explosions.
Product
McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2587-2024·2024-08-28
ClotTriever XL Catheter instructions updated to prevent device entrapment and embolism
Inari Medical has updated instructions for the ClotTriever XL Catheter (30 mm) to prevent device entrapment and pulmonary embolism. Approximately 2,488 units distributed worldwide are affected.
Product
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0638-2024·2024-08-28
FDA Class I Recall: B. Braun Sodium Chloride Injection for Particulate Matter
B. Braun Medical Inc. is recalling 63,444 containers of 0.9% Sodium Chloride Injection USP nationwide due to the presence of particulate matter. This intravenous medication may pose a serious health risk if administered to patients.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V643000·2024-08-28
Volkswagen ID.4 passenger airbag inflator fasteners may be loose
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the fasteners securing the passenger frontal airbag inflator may be loose, so the airbag may not deploy as intended.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2637-2024·2024-08-28
McGRATH MAC EMS Video Laryngoscope Battery Management System Recall
Covidien is recalling McGRATH MAC EMS Video Laryngoscopes due to a battery management system defect that may deplete below design specifications, creating risk of thermal events and explosion. About 10,449 units were distributed worldwide.
Product
McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2701-2024·2024-08-28
Medline medical procedure kits recalled for dimensional variation
Medline is recalling medical procedure kits due to a slight dimensional variation that may cause fitting difficulties. No injuries or illnesses have been reported.
Product
Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET UP, REF DYNJ902752C, b) KIT ENDO, REF DYKE1872A, c) LOWER ENDO KIT, REF DYKE1921A, d) PACEMAKER, REF DYNJ901681D, e) UPPER ENDO KIT, REF DYKE1922A, f) VASCULAR, REF DYNJ905515D, g) VASCUALR,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2686-2024·2024-08-28
Diagnostic Test Kit May Produce False Results in Tuberculosis Drug Resistance Testing
The BD BACTEC MGIT 960 PZA Kit may intermittently produce falsely resistant results when testing TB susceptibility to pyrazinamide. This Class II recall affects 12,383 units distributed worldwide.
Product
BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA) Catalog Number: 245128
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2682-2024·2024-08-28
BIOFIRE FILMARRAY Pneumonia Panel Recalled for Manufacturing Defect
BioFire Diagnostics is recalling 58 units of BIOFIRE FILMARRAY Pneumonia Panel due to a manufacturing defect that increases the risk of control failures and delayed test results.
Product
BIOFIRE FILMARRAY Pneumonia Panel, REF: RFIT-ASY-0144
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2649-2024·2024-08-28
Alcon ClearCut S Ophthalmic Knives Recalled for Sharpness Complaints
Alcon is recalling ClearCut S and A-OK ophthalmic surgical knives due to increased complaint reports about sharpness. Approximately 5,039 units were distributed nationwide and internationally.
Product
Product Desc: Product Name: ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2662-2024·2024-08-28
Alcon recalls ClearCut ophthalmic knives due to sharpness issues
Alcon is recalling approximately 11,916 ClearCut SB Intrepid 2.2 ANG ophthalmic knives due to complaints about blade sharpness. The affected units were distributed nationwide and internationally.
Product
Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number: 8065992245 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2658-2024·2024-08-28
Alcon ClearCut and A-OK Ophthalmic Knives Recalled for Reduced Sharpness
Alcon is recalling ClearCut Sideport and A-OK Corneal/Scleral V-Lance ophthalmic knives due to reports of reduced blade sharpness. The recall affects 6,020 units distributed in the United States and internationally.
Product
Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065982465 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2666-2024·2024-08-28
Alcon ophthalmic surgical knives recalled for sharpness defect
Alcon is recalling 145,248 ophthalmic knives (CLEARCUT SATINSLIT model 8065992745) due to increased complaint reports of inadequate sharpness. The surgical instruments were distributed nationwide and internationally.
Product
Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE2.75MM AN Model/Catalog Number: 8065992745 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2650-2024·2024-08-28
Ophthalmic Knives Recalled Due to Complaints About Reduced Sharpness
Alcon is recalling ophthalmic knives for increased complaints of reduced sharpness. These surgical instruments require consistent blade sharpness for surgical precision in eye procedures.
Product
Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB,2.2 Model/Catalog Number: 8065772245 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide