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.

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.

6026–6050 of 77413

  • SevereCPSC·25390·2025-07-17

    iStore magnetic wireless power banks can overheat and ignite while charging

    iStore Magnetic Wireless Power Banks, model IST-09991/W05, are being recalled because the lithium-ion battery can overheat and ignite while charging. Three incidents and about $15,000 in property damage reported.

    Product
    iStore Magnetic Wireless Power Banks (IST-09991/W05 model only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25391·2025-07-17

    VIVI e-bike lithium-ion batteries can overheat, posing fire and burn hazards

    36-volt lithium-ion batteries supplied with certain VIVI e-bikes are being recalled because they can overheat. Fourteen overheating incidents including three fires have been reported. About 24,000 units affected.

    Product
    36-volt lithium-ion batteries used with VIVI E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25387·2025-07-17

    Traveller aluminum loading ramps can bend or break under rated loads

    Traveller aluminum loading ramps are being recalled because they cannot withstand the weight specified on the ramps and can bend or break in use. Two injuries have been reported. About 18,000 units affected.

    Product
    Traveller Aluminum Loading Ramps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25388·2025-07-17

    Primark Stitch scented highlighters contain phthalates above the federal ban

    Primark DTR Stitch Scented Highlighters 4-packs are being recalled because they contain phthalates in violation of the federal phthalates ban. About 2,600 units are affected.

    Product
    Primark DTR (direct-to-retail) Stitch Scented Highlighters (4-pack)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25392·2025-07-17

    Babyletto Kiwi recliner USB modules can overheat and spark in use

    Babyletto Kiwi Electronic Recliner and Swivel Gliders are being recalled because the USB module in the recliner arm can overheat and spark. About 9,030 units are affected.

    Product
    Babyletto Kiwi Electronic Recliner and Swivel Gliders with USB port
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V474000·2025-07-17

    Genesis G90 and GV60 instrument panel display can fail

    Hyundai is recalling certain 2023-2025 Genesis G90 and GV60 vehicles because a software error may cause the instrument panel display to fail, failing FMVSS 101.

    Product
    GENESIS — GENESIS G90, GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V472000·2025-07-17

    Jeep Grand Cherokee second-row head restraints may not lock upright

    Chrysler is recalling certain 2023-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because the second-row head restraints may not lock in the upright position, failing FMVSS 202.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E044000·2025-07-17

    Chrysler Recalls Mopar Second-Row Head Restraints for Locking Defect

    Chrysler is recalling Mopar second-row head restraints that may not lock in the upright position, increasing injury risk during a crash.

    Product
    SEATS:MID/REAR ASSEMBLY:HEAD RESTRAINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V471000·2025-07-17

    Chrysler Pacifica built with wrong radio may not show rearview image

    Chrysler is recalling certain 2024-2025 Pacifica vehicles that were built with an incorrect radio, which can prevent the rearview camera image displaying. All affected vehicles have been repaired.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2083-2025·2025-07-16

    FEM-FLEX II femoral arterial cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0215-2025·2025-07-16

    Weaver bulk semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.

    Product
    Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2047-2025·2025-07-16

    Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction

    The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.

    Product
    Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2084-2025·2025-07-16

    FEM-FLEX II FEMII018A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2085-2025·2025-07-16

    FEM-FLEX II FEMII018AS cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018AS, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 558 units affected.

    Product
    Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS Software Version: N/A Product Description: The Edwards FEMFLEXII Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0213-2025·2025-07-16

    JLM dark chocolate nonpareils recalled over undeclared milk allergen

    JLM Manufacturing Dark Chocolate Nonpareils in 14 oz tubs are being recalled because of undeclared milk. 971 cases are affected, distributed nationwide.

    Product
    JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0216-2025·2025-07-16

    Weaver white seed nonpareil chocolate recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate (White Seeds) in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 1,760 cases are affected.

    Product
    Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate (White Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2082-2025·2025-07-16

    FEM-FLEX II FEMII016A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII016A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 6,801 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2080-2025·2025-07-16

    Optisite OPTI16 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI16 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 27,022 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V470000·2025-07-16

    BMW electric vehicle battery modules may be improperly assembled

    BMW is recalling certain 2022-2025 iX, 2023-2024 i7 and 2022-2023 i4 vehicles because high-voltage battery cell modules may not have been assembled properly, stressing the module frame.

    Product
    BMW — BMW IX, I7, I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2025·2025-07-16

    Nuclear medicine systems may show unintended radial detector motion during scans

    Varicam, Millennium VG, Millennium VG Hawkeye and Discovery VH nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software version. 21 units affected.

    Product
    Varicam, Millennium VG, Millennium VG Hawkeye, Discovery VH Nuclear Medicine System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2025·2025-07-16

    VersaCross access kits may have a hole in the sterile pouch

    VersaCross Access Solution 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 Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF WIRE 63CM/45DEG/D1) VXSK0102 VXSK (180J RF WIRE 63CM/55DEG/D0) VXSK0103 VXSK (180P RF WIRE 63CM/45DEG/D0) VXSK0121 VXSK (180P RF WIRE 63CM/45DEG/D1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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