The Recall Desk

State

New Hampshire product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6051–6075 of 77413

  • HighFDA (Devices)·Z-2109-2025·2025-07-16

    Alcon Constellation procedure packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Combined Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 89,495 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Combined Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2110-2025·2025-07-16

    Alcon Custom Pak surgical kits may have damaged lidding compromising sterility

    Alcon Custom Paks, customer-designed sterile surgical kits, are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 15,557 kits affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience kits intende
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2105-2025·2025-07-16

    VersaCross transseptal sheath kits may have a punctured sterile barrier pouch

    VersaCross Transseptal Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS 63CM/45DEG/D0 SHEATH VXS2112 VERSACROSS SHEATH (63CM 45DEG D0)-J Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, includ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2106-2025·2025-07-16

    Torflex transseptal guiding sheath kits may have a punctured sterile pouch

    Torflex Transseptal Guiding Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2101-2025·2025-07-16

    O-arm O2 imaging system gantry support may have been damaged

    The O-arm O2 Imaging System is being recalled because a mechanical component supporting the gantry to the support structure may have been damaged during manufacture. 3 units affected.

    Product
    O-arm O2 Imaging System. Mobile X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2025·2025-07-16

    VersaCross RF wire lots may have a punctured sterile barrier pouch

    The VersaCross RF Wire is being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units are affected.

    Product
    VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device approved and commercialized in Japan only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2108-2025·2025-07-16

    Alcon Constellation vitrectomy packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2025·2025-07-16

    Preat Astra dental analogs have rotational feature 180 degrees off

    Preat Astra EV-compatible 4.2 mm Digital Analogs are being recalled because a manufacturing error left the digital analog rotational feature 180 degrees off. 44 units are affected.

    Product
    Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2091-2025·2025-07-16

    TrueDent Cyan dental resin cartridges carry an expiration date formatting error

    TrueDent Cyan dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 100 units are affected.

    Product
    TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2092-2025·2025-07-16

    TrueDent dental resin cartridges carry a formatting error in expiration dates

    TrueDent Magenta dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 94 units are affected.

    Product
    TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2093-2025·2025-07-16

    TrueDent Yellow dental resin cartridges carry an expiration date formatting error

    TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.

    Product
    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2094-2025·2025-07-16

    TrueDent White dental resin cartridges carry an expiration date formatting error

    TrueDent White dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 109 units are affected.

    Product
    TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0509-2025·2025-07-16

    Famciclovir tablets recalled after a hair was found on a tablet

    Famciclovir Tablets USP 500 mg from Macleods Pharma are being recalled because a black hair strand was found attached to a tablet in a sealed bottle. 9,888 bottles are affected.

    Product
    FAMCICLOVIR — FAMCICLOVIR (FAMCICLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2090-2025·2025-07-16

    TrueDent Clear dental resin cartridges carry an expiration date formatting error

    TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.

    Product
    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V415000·2025-07-15

    Porsche suspension strut retaining ring can loosen dislodging the strut

    Porsche is recalling certain 2025 Panamera, Panamera E-Hybrid and Taycan vehicles because a retaining ring on top of the suspension strut may come loose, dislodging the strut and losing air from the spring.

    Product
    PORSCHE — PORSCHE TAYCAN, PANAMERA, PANAMERA 4 E-HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V408000·2025-07-15

    Winnebago Recalls 2025 Micro Minnie Trailers Due to Cooktop Flame Inversion Risk

    Winnebago is recalling 2025 Micro Minnie and Micro Minnie FLX travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE FLX, MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V468000·2025-07-14

    AMO Recalls 2025 Utility Trailers Due to Axle Separation Risk

    American Manufacturing Operations is recalling 2025 AMO Utility trailers because shackle nuts may loosen, allowing the axle to detach and increasing crash risk.

    Product
    AMO — AMO UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E043000·2025-07-14

    Peragon Tectonic Tonneau Covers Recalled for Detachment Risk

    Peragon is recalling Tectonic hard tonneau covers because damaged plastic slides may allow the cover to detach during transit, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V420000·2025-07-14

    Polestar 3 panoramic glass sunroofs may not be properly secured

    Polestar is recalling certain 2025 Polestar 3 vehicles because the panoramic glass sunroof may not be properly secured and can detach. 33 vehicles are affected.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V459000·2025-07-11

    Zero Motorcycles Recalls 2024 Models Due to Front Brake Hose Defect

    Zero Motorcycles is recalling 2024 DSR/X, DS, DSR, and DSRP motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.

    Product
    ZERO — ZERO DSRP, DSR, DS, DSR/X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V467000·2025-07-11

    Ford Bronco Sport and Escape fuel injectors may crack and leak

    Ford is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles with 1.5L engines because a fuel injector may crack and leak fuel inside the engine compartment. 694,271 vehicles affected.

    Product
    FORD — FORD BRONCO SPORT, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V463000·2025-07-11

    Mercedes-Benz Metris rearview camera image may fail to display

    Daimler Vans USA is recalling certain 2020-2023 Mercedes-Benz Metris vehicles because unsecured infotainment connections can stop the rearview camera image displaying. 43,422 vehicles affected.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide