State

New Hampshire product recalls

72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8026–8050 of 77430

ModerateFDA (Devices)·Z-1042-2025·2025-02-05
Medline procedure kits recalled for surgical mask bioburden contamination risk
Medline procedure kits containing surgical masks are recalled nationwide because included masks failed to meet bioburden testing standards, creating potential infection risk during medical procedures.
Product
Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT, Reorder number DYNDC3189; dressing change tray
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V054000·2025-02-04
Highland Ridge Recalls 2025 Open Range 3X Trailers for Incorrect Tire Labeling
Highland Ridge RV is recalling 2025 Open Range 3X fifth-wheel travel trailers because the vehicle certification label lists the wrong tire size, which could lead to incorrect tire installation.
Product
HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE 3X
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V052000·2025-02-03
Temsa Recalls 2024 TS35 Vehicles Due to Fuel Hose Separation Risk
Temsa is recalling 2024 TS35 vehicles with Cummins L9 engines because fuel filter hoses may separate, causing leaks, engine stalls, and fire or crash risks.
Product
TEMSA — TEMSA TS35
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V053000·2025-02-03
New Flyer Transit Buses Recalled for Fuel Hose Separation Risk
New Flyer is recalling 210 transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.
Product
NEW FLYER — NEW FLYER XDE60, XD35, XD40, XD60
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V049000·2025-01-31
Ford Recalls 2025 Models for Instrument Panel Illumination Defect
Ford is recalling 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles because the instrument panel may fail to illuminate, increasing crash risk.
Product
LINCOLN — LINCOLN, FORD CORSAIR, ESCAPE, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V051000·2025-01-31
Roadtrek Recalls Westfalia Wave Vans Due to Incorrect Weight Labels
Roadtrek is recalling 2023-2025 Westfalia Wave Pop Top vans because incorrect weight labels may lead to unintentional overloading and increased crash risk.
Product
ROADTREK — ROADTREK WESTFALIA WAVE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V048000·2025-01-31
Ford and Lincoln rearview cameras may show blank or distorted images
Ford is recalling certain 2021 Expedition, 2021-2022 Super Duty F-250 to F-600 and 2020-2022 Lincoln Corsair vehicles because the rearview camera may display a blank or distorted image.
Product
FORD — FORD, LINCOLN F-250 SD, F-550 SD, F-450 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V045000·2025-01-30
Autocar Recalls 2023-2025 E-ACTT Vehicles Due to Software Error
Autocar is recalling 2023-2025 E-ACTT vehicles because a software error may cause the vehicle to roll away on an incline or stall the engine.
Product
AUTOCAR — AUTOCAR E-ACTT
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25114·2025-01-30
Portable Folding Stadium Seats Recalled Due to Fall and Injury Hazards
AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.
Product
AMX Global Portable Folding Stadium Seats
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25113·2025-01-30
Girls pajamas recalled due to flammability regulation violation, burn-injury risk
Cozchique, Tebbis, and Beeziac girls pajamas sold on Amazon violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. About 6,050 units distributed May through September 2024.
Product
Cozchique, Tebbis and Beeziac Girls Pajamas
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25109·2025-01-30
Matrix-brand Training Cycles Recalled Due to Unexpected Seat Collapse
Johnson Health Tech North America is recalling approximately 12,885 Matrix-brand Training Cycles due to seats that can unexpectedly lower during use. The company received 63 reports, including two falls, but no injuries have been reported.
Product
Matrix-brand Training Cycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25115·2025-01-30
Pearhead Infant Learning Toy Sets Recalled for Choking Hazard in Rattle
Pearhead Infant Learning Toy Sets are recalled because the wooden egg-shaped rattle can lodge in a child's throat, creating a choking hazard. The recall affects about 2,700 units sold from August through October 2024.
Product
Pearhead Infant Learning Toy Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25112·2025-01-30
Hair Dryers Recalled for Missing Immersion Protection, Electrocution Risk
AliExpress is recalling about 980 Multi Styler Hair Dryers sold online from May 2023 through November 2024 because they lack an immersion protection device and pose an electrocution hazard if they fall into water while plugged in.
Product
6-in-1 Multi Styler and 5-in-1 Multi Styler Hair Dryers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25111·2025-01-30
Digital Kitchen Scales Recalled for Coin Battery Ingestion Risk
Greater Goods digital kitchen scales with easily accessible lithium coin batteries violate federal safety regulations due to missing child-resistant packaging and warnings. Ingestion of coin batteries can cause serious injury or death; no incidents have been reported.
Product
Greater Goods Digital Kitchen Scales
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25110·2025-01-30
Cabinet Health 4 oz. Refillable Medicine Bottles Recalled for Degrading Lids
Cabinet Health is recalling about 65,000 refillable 4 oz. medicine bottles. The plastic lids can degrade with repeated use, losing child-resistance and posing a poisoning risk if children access the contents.
Product
Cabinet Health 4 oz. Refillable Medicine Bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V042000·2025-01-30
Brinkley fifth wheel solar charge controllers can fail and overheat
Brinkley RV is recalling certain 2024-2025 Model G fifth wheel trailers because the solar charge controller may fail and overheat, increasing the risk of fire.
Product
BRINKLEY RV — BRINKLEY RV MODEL G
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V044000·2025-01-30
Autocar Recalls 2024-2025 Xpeditor Vehicles Due to Radar Software Error
Autocar is recalling 2024-2025 Xpeditor vehicles because a software error may cause the forward collision sensing radar to fail, increasing crash risk.
Product
AUTOCAR — AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V043000·2025-01-30
Jayco Recalls 2025 Jay Feather Micro Trailers Due to Gas Leak Risk
Jayco is recalling 2025 Jay Feather Micro trailers because a cracked burner tube may cause a gas leak, increasing fire risk.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FEATHER MICRO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V040000·2025-01-29
Toyota and Lexus spiral cable fault can deactivate the driver airbag
Toyota is recalling certain 2023-2024 Toyota and Lexus vehicles that may have been incorrectly repaired under recall 23V-480, because an insufficiently welded connection can deactivate the driver's airbag.
Product
LEXUS — LEXUS, TOYOTA RX, HIGHLANDER, COROLLA, NX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0960-2025·2025-01-29
VDR4 Phasitron Breathing Circuit Recalled for Potential Ventilation Reduction
Percussionaire Corporation is recalling VDR4 Phasitron breathing circuit models due to a venturi component that may stick and reduce ventilation. This Class I recall affects over 4,700 units worldwide.
Product
VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk -A51001, VDR4 Control Unit Tester -PRT 991, VDR W/SWIVEL T SINGLE PATIENT PHASITRON -PRT 992, VDR4 HUMIDIFICATION ADAPTER KIT, CASE OF 10 -PRT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0207-2025·2025-01-29
FOUZEE SugarLin Herbal Formula Capsules Recalled for Undeclared Prescription Drugs
Shoppers-Plaza is recalling FOUZEE SugarLin Herbal Formula capsules because FDA testing found undeclared metformin and glyburide. The product was marketed without FDA approval.
Product
FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of India. UPC 8 26656 69047 7
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1011-2025·2025-01-29
Baxter Continu-Flo Solution Set with Duo-Vent Spike recalled for inverted clamps
Baxter is recalling specific lots of Continu-Flo Solution Sets due to potentially inverted side clamps that render the tubing unusable. Distribution included eight US states.
Product
Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2025·2025-01-29
Otological Ventilation Tubes Recalled for Missing FDA 510(k) Clearance
Adept Medical Ltd is recalling 13,070 Otological Ventilation Tubes because they were distributed without FDA 510(k) clearance. Over 9,000 units were distributed in the US and 3,980 internationally.
Product
Otological Ventilation Tube - T-Tube 6mm - Silicone; Product Code: NZ3306/NZ3306-2;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0966-2025·2025-01-29
Otological Ventilation Tubes Recalled for Lack of FDA Premarket Clearance
Adept Medical Ltd is recalling Otological Ventilation Tubes (T-Tube 9mm, Silicone) distributed without FDA 510(k) premarket notification clearance. Approximately 6,280 units were distributed in the US and internationally.
Product
Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1014-2025·2025-01-29
Dressing Change Kits Recalled for Potential Package Sterility Compromise
Trinity Sterile is recalling Wolf-Pak Dressing Change Kits due to a potential hole in the package that could compromise the sterility of the medical kit. Lot #600022 (3,960 units) distributed nationwide.
Product
Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Border Tegaderm Dressing & 3mL CHG One Step Applicator CS/30 Model/Catalog Number: DC3080LF Software Version: N/A Product Description: Dressing change kit, case of 30, lot #600022, 132 cases affected. Componen
Category
Medical Device
Distribution
Distributed nationwide