State

New Hampshire product recalls

72,936 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.

Which agencies issued them

These figures cover only the 4,444 recalls whose distribution notice names New Hampshire specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3251–3275 of 77380

ModerateFDA (Devices)·Z-1343-2026·2026-02-18
Spinal navigation instruments recalled over incorrect array connection geometry
Alphatec Spine is recalling 15 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Product
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1342-2026·2026-02-18
Navigation osteotomes recalled over incorrect array connection geometry
Alphatec Spine is recalling 7 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Product
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1361-2026·2026-02-18
Display adapters recalled after the wrong configuration file was used
Steris is recalling 10 units of the Barco MNA with HexaVue IP Integration System because the supplier used the incorrect configuration file for a limited batch of adapter components.
Product
Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0303-2026·2026-02-18
Sensitive skin numbing spray recalled over manufacturing practice deviations
Pro Numb Tattoo Numbing Spray LLC is recalling Pro Numb Tattoo Numbing Spray For Sensitive Skin, 4% Lidocaine, over cGMP deviations.
Product
PRO NUMB SENSITIVE SKIN — PRO NUMB SENSITIVE SKIN (NUMBING SPRAY)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1341-2026·2026-02-18
Compact suction units recalled over electromagnetic noise above aviation limits
Laerdal Medical is recalling 1,202 Compact Suction Unit 4 RTCA units because those made in a limited period may emit electromagnetic noise beyond the acceptable RTCA limits.
Product
Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052; 2) LCSU 4, 300 ml, RTCA; Catalog Number: 880062; 3) LCSU 4, RTCA; Catalog Number: 881152;
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1358-2026·2026-02-18
Newborn monitor caps recalled over an incorrect sizing guide on labeling
SurePulse Medical is recalling the Surepulse VS Cap Medium because the labeling contains an incorrect sizing guide for the cap.
Product
Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1337-2026·2026-02-18
Dental impression posts recalled over caps in the wrong colour
Straumann USA is recalling 561 WB Impression Post Closed Tray units because the impression caps provided in the package are magenta instead of brown.
Product
WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1359-2026·2026-02-18
Large newborn monitor caps recalled over an incorrect sizing guide
SurePulse Medical is recalling the Surepulse VS Cap Large because the labeling contains an incorrect sizing guide for the cap.
Product
Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1357-2026·2026-02-18
Small newborn monitor caps recalled over an incorrect sizing guide
SurePulse Medical is recalling the Surepulse VS Cap Small because the labeling contains an incorrect sizing guide for the cap.
Product
Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1360-2026·2026-02-18
Extra large newborn monitor caps recalled over an incorrect sizing guide
SurePulse Medical is recalling the Surepulse VS Cap Extra Large because the labeling contains an incorrect sizing guide for the cap.
Product
Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1356-2026·2026-02-18
Extra small newborn monitor caps recalled over an incorrect sizing guide
SurePulse Medical is recalling the Surepulse VS Cap Extra Small because the labeling contains an incorrect sizing guide for the cap.
Product
Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V088000·2026-02-17
Blue Arc BA4L-800 Recalled for Steering Gearbox Mounting Defect
Shyft Group is recalling 2024-2025 Blue Arc BA4L-800 vehicles because steering gearbox mounting fasteners may loosen, causing the gearbox to bind and increasing crash risk.
Product
BLUE ARC — BLUE ARC BA4L-800
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V093000·2026-02-17
Prevost Recalls 2025-2026 X3-45 Buses Due to Seat Anchor Defect
Prevost is recalling 2025-2026 X3-45 commuter buses because improperly installed seat anchors may not restrain occupants during a crash.
Product
PREVOST — PREVOST X3-45 COMMUTER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V089000·2026-02-17
Winnebago View and Navion rear roof cap trim may detach
Winnebago is recalling certain 2020-2023 View and Navion recreational vehicles because the rear roof cap aerofence trim may become loose and detach during transit.
Product
WINNEBAGO — WINNEBAGO VIEW, NAVION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V091000·2026-02-17
Ford Escape and Lincoln Corsair plug-in hybrid battery cells may short
Ford is recalling certain 2022-2026 Escape and 2023-2026 Lincoln Corsair plug-in hybrids because a defect in one or more high voltage battery cells may cause an internal short circuit and battery failure.
Product
FORD — FORD, LINCOLN ESCAPE PHEV, CORSAIR PHEV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V090000·2026-02-17
Ford Recalls 2025 Transit Vehicles for Brake Pedal Disconnection Risk
Ford is recalling 2025 Transit vehicles because the brake pedal may disconnect from the booster pushrod, causing a loss of brake function and increasing crash risk.
Product
FORD — FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V085000·2026-02-13
Chevrolet, GMC and Cadillac transmission control valve may lock rear wheels
GM is recalling certain 2022 Tahoe, Suburban, Yukon, Yukon XL, Escalade and Escalade ESV vehicles with the 10-speed ETRS transmission because the transmission control valve may fail and lock up the rear wheels.
Product
CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, TAHOE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E007000·2026-02-13
Couture Hyperax Volt RV 4x Bike Carrier Recall for Detachment Risk
Couture Co Ltd is recalling Hyperax Volt RV 4x bike carriers because vibrations may cause anchoring plates to fail, allowing the carrier or bike to detach from the vehicle.
Product
EQUIPMENT:MECHANICAL:CARRIER/RACK recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V087000·2026-02-13
Thomas Built Buses Recalling Saf-T-Liner Models for Heater Hose Clamp Defect
Daimler Trucks North America is recalling 2023-2026 Thomas Built Buses Saf-T-Liner EFX and HDX models because improperly tightened heater hose clamps may cause hot coolant to leak into the passenger compartment.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V086000·2026-02-13
Thomas Built Buses Recalls 2023-2026 Models for Heater Hose Clamp Defect
Daimler Trucks North America is recalling 2,843 Thomas Built Buses Saf-T-Liner EFX and HDX school buses because improperly tightened heater hose clamps may cause hot coolant to leak inside the passenger compartment.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V083000·2026-02-12
Chevrolet and GMC transmission control valve failure may lock rear wheels
GM is recalling certain Chevrolet Silverado and GMC Sierra vehicles that may have been repaired incorrectly under recall 24V797, because the transmission control valve may fail and lock the rear wheels.
Product
CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500, SILVERADO 2500, SILVERADO 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V084000·2026-02-12
International truck software may fail to brake with adaptive cruise
International is recalling certain 2026-2027 MV vehicles because the ECU software may fail to engage the brakes when adaptive cruise control or hill hold assist is in use.
Product
INTERNATIONAL — INTERNATIONAL MV
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V082000·2026-02-12
Cadillac Lyriq rearview camera screen may turn gray without image
GM is recalling certain 2024 Cadillac Lyriq vehicles because the rearview camera screen may turn gray with no camera image.
Product
CADILLAC — CADILLAC LYRIQ
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·26265·2026-02-12
Magnetic board games recalled over loose high-powered magnet pieces
About 1,200 Colombia-themed magnetic board games are being recalled because the magnetic game pieces contain loose high-powered magnets, posing an ingestion hazard to children.
Product
Colombia-themed Magnetic Board Games
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26268·2026-02-12
Spa hydromassage jets recalled over hair entanglement and drowning hazards
About 32,900 hydromassage rotary jets in Highlife Collection spas are being recalled because the suction force can entangle a user's hair and submerge their head underwater.
Product
Hydromassage Rotary Jet (6 fin) in Highlife Collection spas
Category
Consumer Product
Distribution
Distributed nationwide