State

New Hampshire product recalls

72,913 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 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2001–2025 of 77357

ModerateFDA (Devices)·Z-2111-2026·2026-05-13
Medline Convenience Kits recalled due to sterilization calibration issues
Medline Industries has recalled 6,676 units of multiple Medline Convenience Kits used in gynecological and other surgical procedures due to calibration issues with sterilization equipment that may affect sterility assurance.
Product
Medline Convenience Kits: 1) HYSTEROSCOPY, Model Number: CDS984086I; 2) KIT GYN ONCOLOGY LAP, Model Number: DYKMBNDL91A; 3) VAGINAL HYSTERECTOMY PACK-LF, Model Number: DYNJ0373807J; 4) VAGINAL HYSTERECTOMY PACK-LF, Model Number: DYNJ0373807K; 5) D&C/HYSTEROSCOPY PACK, Mo
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2117-2026·2026-05-13
Medline Convenience Kits recalled due to sterilization calibration issues
Medline Industries is recalling two models of gastrointestinal convenience kits (BAPTIST FLOYD ENDO GI KIT and GI LAB OTHER ENDO KIT) due to calibration issues in sterilization equipment that may have impacted the sterility assurance level of the products.
Product
Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT, Model Number: DYKE1455B; 2) GI LAB OTHER ENDO KIT, Model Number: DYKE1721
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2077-2026·2026-05-13
DEX Ophthalmic Tissue Forceps Require Corrective Instructions Update
Katalyst Surgical is correcting instructions for DEX Ophthalmic Tissue Forceps (Model DVF4022-25-S) due to a field safety issue related to the Instructions for Use (IFU).
Product
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2083-2026·2026-05-13
One Step UTI in vitro diagnostic test recalled for missing FDA approval
DFI Co., Ltd. is recalling the One Step UTI in vitro diagnostic test (REF: 3374) because it was distributed without required FDA premarket clearance or approval.
Product
One Step UTI in vitro diagnostic test REF: 3374
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2086-2026·2026-05-13
Uric Acid in vitro diagnostic test distributed without FDA clearance
DFI Co., Ltd. is recalling its Uric Acid in vitro diagnostic test (REF: 31H0P) because the devices were distributed without required FDA premarket clearance or approval.
Product
Uric Acid in vitro diagnostic test REF: 31H0P
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2115-2026·2026-05-13
Medline Tracheostomy Convenience Kits Sterilization Calibration Recall
Medline Industries is recalling certain tracheostomy convenience kits and related products due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY, Model Number:DYKMBNDL55; 2) KIT STC TRACHEOSTOMY, Model Number:DYKMBNDL55A; 3) TRACH TOTE, Model Number:DYNJ85691
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2112-2026·2026-05-13
Medline Surgical Convenience Kits Recalled Due to Sterilization Calibration Issues
Medline Industries has recalled multiple surgical convenience kits after discovering calibration issues with sterilization equipment that may impact the sterility assurance level of the devices. The kits include robotic surgery, gynecology, urology, and general surgical packs distributed nationwide.
Product
Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS, Model Number: CDS982407N; 2) BAP NORTH ROBOTIC SURGERY CDS, Model Number: CDS982407N; 3) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431J; 4) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431K; 5) TOT/ GYN LITHOTO
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0511-2026·2026-05-13
Buspirone Hydrochloride Tablets 5 mg Recalled for Subpotency
Unichem Pharmaceuticals USA Inc. is recalling Buspirone Hydrochloride Tablets, USP, 5 mg because the drug is subpotent. The recall affects approximately 10,875 bottles distributed nationwide.
Product
BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V299000·2026-05-12
Ford Bronco hardtop roof panel sections may separate and detach
Ford is recalling certain 2021-2022 Bronco vehicles because Molded-In-Color hardtop roof panels may have been manufactured improperly, allowing outer sections to detach.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V297000·2026-05-12
2026 Land Rover Range Rover vehicles recalled for faulty seat belt warning
Jaguar Land Rover is recalling certain 2026 Range Rover Velar, Range Rover Sport, and Range Rover vehicles because the seat belt warning chime may not sound when occupants are unbuckled, increasing crash injury risk.
Product
LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER VELAR, RANGE ROVER SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V301000·2026-05-12
Ford Recalls 2026 Escape and Lincoln Corsair for Park Module Failure
Ford is recalling 2026 Escape and Lincoln Corsair vehicles because the park module may fail to lock, increasing the risk of the vehicle rolling away and causing a crash.
Product
LINCOLN — LINCOLN, FORD CORSAIR, ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V302000·2026-05-12
Vespa Motorcycles Recalled for Missing Rearview Mirror Warning Label
Piaggio Group Americas is recalling 285 specific Vespa models because the rearview mirrors lack the required convex mirror warning text.
Product
VESPA — VESPA GTV 310, PRIMAVERA 150, PRIMAVERA 50
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E029000·2026-05-12
Hiab Recalls Waltco MDV Series Liftgates Due to Deck Pin Failure Risk
Hiab USA Inc. is recalling certain Waltco MDV series liftgates because deck pins may break, causing the platform to fall and increasing injury risk.
Product
STRUCTURE:BODY:HATCHBACK/LIFTGATE:HINGE AND ATTACHMENTS recall
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·26V300000·2026-05-12
Nova Bus speaker hole doors are missing the glazing DOT mark
Nova Bus is recalling certain LFS transit buses because the driver's speaker hole door may lack the prime glazing manufacturer DOT code mark, breaching FMVSS 205.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V294000·2026-05-11
International Recalls 2026-2027 HV Trucks for Brake Release Delay
International is recalling 2026-2027 HV vehicles because the service brake may take longer than expected to release, increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL HV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E028000·2026-05-11
Beck/Arnley Replacement Lower Control Arm and Ball Joint Recall
Federal-Mogul Motorparts is recalling Beck/Arnley replacement lower control arm and ball joint assemblies for 2018-2025 Subaru Forester and Crosstrek vehicles due to loose nuts.
Product
SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V295000·2026-05-11
Forest River Recalls 2026 Prime Time Crusader Trailers for Sewer Gas Risk
Forest River is recalling 2026 Prime Time Crusader recreational trailers because the waste water ventilation pipe may end inside the trailer, allowing sewer gas to enter the cabin.
Product
PRIME TIME — PRIME TIME CRUSADER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V296000·2026-05-11
2024 Chrysler Pacifica wheelchair restraints may not lock properly
Braun Corporation is recalling certain 2023–2026 Chrysler Pacifica vehicles because wheelchair retractors may not lock, preventing proper securement. An unsecured wheelchair can move during transit and increase injury risk.
Product
CHRYSLER — CHRYSLER PACIFICA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V293000·2026-05-08
Fly Wing Snake 250 EFI Motorcycles Recalled for Brake Pad Defect
NHTSA is recalling 2024 Fly Wing Snake 250 EFI motorcycles because brake pads may fail in wet conditions, increasing crash risk.
Product
FLY WING — FLY WING SNAKE 250 EFI
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E027000·2026-05-08
Dometic Recalls Fan-Tastic Vent Fans Due to Missing Hinge Pin
Dometic is recalling specific Fan-Tastic Vent Fans because a missing hinge pin allows the lid to detach, creating a road hazard for other vehicles.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V292000·2026-05-08
Shyft Recalls Spartan RV Chassis Vehicles Due to Brake Light Defect
Shyft Group is recalling specific Spartan RV chassis vehicles because the exterior brake lights may remain illuminated when the brakes are not applied, increasing crash risk.
Product
SPARTAN — SPARTAN RV CHASSIS K3, RV CHASSIS K2, RV CHASSIS K4, RV CHASSIS K1
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·26465·2026-05-07
EEMB Lithium Battery Packs Recalled for Unsafe Child-Resistant Packaging
EEMB lithium coin battery packs sold online are not in child-resistant packaging as required by law. If swallowed by a child, these batteries can cause serious internal injuries or death.
Product
EEMB Lithium Battery Packs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26468·2026-05-07
Svnntaa Bed Rails Recalled Due to Entrapment and Asphyxiation Risk
Svnntaa bed rails sold on Amazon violate safety standards and pose a risk of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact Eokeanon for a refund.
Product
Svnntaa Bed Rails
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·26V288000·2026-05-07
RAM Recalls 2023-2026 Ram 2500 Trucks for Software Error
Chrysler is recalling 2023-2026 Ram 2500 trucks because a software error may allow vehicle speed to exceed tire ratings, risking loss of control.
Product
RAM — RAM 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26475·2026-05-07
Analemma Water Bottles recalled for laceration and ingestion hazards
Analemma Water Bottles are recalled because the inner glass liner can break, posing risk of serious injury or death from laceration and ingestion. The importer has received 20 reports of the glass breaking, including one oral injury.
Product
Analemma Water Bottles
Category
Consumer Product
Distribution
Distributed nationwide