The Recall Desk

State

New Hampshire product recalls

73,809 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,483
Critical
603
Severe
1,049
Most recent
2026-11-04

Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40076–40100 of 78292

  • HighFDA (Devices)·Z-2341-2018·2018-07-11

    Intuitive Surgical Recalls da Vinci X Systems with Defective Arm Controller Boards

    Intuitive Surgical is recalling 35 da Vinci X Surgical Systems because defective Arm Controller Joint boards have a high rate of failure.

    Product
    da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System (da Vinci X Surgical System Mode IS4200) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments including rigid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V465000·2018-07-11

    BMW and MINI Recall 5,309 Vehicles for Crankshaft Sensor Defect

    BMW is recalling 5,309 vehicles because a crankshaft sensor firmware error may cause the engine to stall, increasing crash risk.

    Product
    MINI — MINI, BMW JCW, X2, COUNTRYMAN, CLUBMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2294-2018·2018-07-11

    Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation

    Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.

    Product
    LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-044
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2357-2018·2018-07-11

    FHC Depth Stop Adapter Recall for Lead Damage Risk

    FHC, Inc. is recalling the microTargeting STar Drive System (Manual) because the Depth Stop Adapter can damage implanted leads if over-tightened, requiring replacement.

    Product
    microTargeting" STar" Drive System (Manual) Distributed by Medtronic, Product Number FC8001
    Category
    Medical Device
    Distribution
    46 states
  • ModerateFDA (Devices)·Z-2334-2018·2018-07-11

    St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recall

    St. Jude Medical is recalling 986 Confirm Rx Insertable Cardiac Monitors because exposure to sub-freezing temperatures caused a transient battery voltage drop, resulting in an incorrect low battery indicator display.

    Product
    St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for the monitoring and diagnostic evaluation of patients who experience unexplained symptoms such as: dizziness, palpitations, chest pain, syncope, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1606-2018·2018-07-11

    Icelandic Provisions Recalls Vanilla Skyr Cups Due to Coconut Mislabeling

    Icelandic Provisions Inc. is recalling Vanilla Skyr cups that may contain coconut skyr yogurt. The recall addresses a labeling error regarding the product flavor.

    Product
    Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-2344-2018·2018-07-11

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products PHYT Slides

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products PHYT Slides due to a potential for imprecise results in quality control and patient samples.

    Product
    VITROS Chemistry Products PHYT Slides, Catalog Number 8298671. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2335-2018·2018-07-11

    St Jude Medical Recalls Merlin PCS Programmer Software for ICM Battery Display Error

    St Jude Medical is recalling Merlin PCS Programmer Software to address an incorrect low battery indicator on Confirm Rx ICM devices caused by supply chain temperature exposure.

    Product
    Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, and for this recall the software that resides on the programmer (software model 3330) is the method of delivery of the new…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0892-2018·2018-07-11

    Qualgen Recalls Estradiol Pellets Due to Incorrect or Missing Lot and Expiration Dates

    Qualgen, LLC is recalling Estradiol 20mg Pellets because the vials have incorrect or missing lot and expiration dates.

    Product
    ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0893-2018·2018-07-11

    Qualgen Recalls Testosterone Pellets Due to Incorrect Lot and Expiration Dates

    Qualgen, LLC is recalling Testosterone 200 mg Pellets because the vials have incorrect or missing lot and expiration dates.

    Product
    TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0907-2018·2018-07-11

    Equate ClearLAX Recalled for Unfiled NDC Numbers on Labeling

    Lupin Somerset is recalling Equate ClearLAX laxative bottles due to unfiled NDC numbers on the labels. This is a Class III recall with no reported health risks.

    Product
    Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic Laxative, OTC, packaged in a) 119 g bottle (NDC 49035-312-07), b) 238 g bottle (NDC 49035-312-08), Distributed by: Wal-mart Stores, Inc., Bentonville, AR 72716
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V458000·2018-07-10

    MV Agusta Recalls 2018 Motorcycles Due to Fork Axle Thread Damage

    MV Agusta is recalling 2018 Brutale 800 Dragster RC, F3 800, and F3 800 RC motorcycles because damaged fork axle threads may cause wheel clamping screw play and loss of control.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RC, F3 800, F3 800 RC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V457000·2018-07-10

    Mercedes-Benz Recalls 2017 AMG G65 for Reverse Speed Software Defect

    Mercedes-Benz is recalling 2017 AMG G65 vehicles because incorrect reverse speed limitation software may cause instability and rollover risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G65
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18185·2018-07-10

    Ortovox Recalls Avalanche Transceivers Due to Software Error

    Ortovox is recalling about 20,000 avalanche transceivers because a software error may prevent them from transmitting survivor location data, delaying rescue efforts.

    Product
    Avalanche transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V452000·2018-07-06

    Nissan Recalls 2007-2008 Versa Models Due to Air Bag Inflator Defect

    Nissan is recalling 2007-2008 Versa sedans and hatchbacks because the passenger air bag inflators may explode. This defect could cause metal fragments to strike occupants, resulting in serious injury or death.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V453000·2018-07-06

    BMW Recalls 2018-2019 X3 and X4 Models for Brake Caliper Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because insufficient coating on rear brake caliper pistons may reduce braking performance.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V446000·2018-07-05

    Entegra Recalls 2019 Motorhomes for Windshield Wiper Defect

    Entegra is recalling 2019 Emblem and Vision motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA EMBLEM, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V449000·2018-07-05

    Jayco Recalls 2019 White Hawk Trailers Due to Ladder Screw Defect

    Jayco is recalling 2019 White Hawk recreational trailers because screws securing ladder steps may break, posing a fall risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V451000·2018-07-05

    Jayco Recalls 2018-2019 Motorhomes Due to Incorrect Cargo Capacity Label

    Jayco is recalling 2018-2019 Alante, Precept, Seneca, Redhawk, and Melbourne motorhomes because the cargo capacity label overstates limits, increasing crash risk.

    Product
    JAYCO — JAYCO PRECEPT, REDHAWK, ALANTE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide