The Recall Desk

State

New Hampshire product recalls

73,576 recalls have nationwide distribution and so reach New Hampshire. 4,477 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,477
Critical
606
Severe
1,045
Most recent
2026-10-21

Of the 4,477 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,045 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,477 recalls whose distribution notice names New Hampshire specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

176–200 of 78053

  • ModerateFDA (Devices)·Z-0084-2027·2026-10-14

    Beckman Coulter DxC 500 AU Clinical Chemistry Analyzers Recalled for Software Error

    Beckman Coulter is recalling DxC 500 AU Clinical Chemistry Analyzers due to a software issue that may cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.

    Product
    DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No. C63519 2. AU w/ISE, Part No. C63520
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0098-2027·2026-10-14

    Avid Medical Recalls Robotic Prostatectomy Packs for Lubricant Contamination

    Avid Medical, Inc. is recalling six Robotic Prostatectomy Packs (NAMC423-11) because they may be contaminated with a manufacturing lubricant.

    Product
    ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0117-2027·2026-10-14

    LeMaitre TufTex Over-the-Wire Embolectomy Catheter Recalled for Balloon Failure

    LeMaitre Vascular, Inc. is recalling 54 TufTex Over-the-Wire Embolectomy Catheters because the balloon components may fail under pull force.

    Product
    TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0104-2027·2026-10-14

    AVID Medical Recalls Major Packs Due to Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 40 Major Packs (Model NIHB0018-11) because they may be contaminated with a lubricant used during manufacturing.

    Product
    MAJOR PACK; Model/Item Number (Kit): NIHB0018-11;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0105-2027·2026-10-14

    AVID Medical Recalls GYN Laparoscopy Packs Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 28 GYN Laparoscopy Packs (Model NAMC436-12) because they may be contaminated with a lubricant used during manufacturing.

    Product
    GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0106-2027·2026-10-14

    AVID Medical Recalls 23 ABD Hysterectomy Kits Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 23 ABD Hysterectomy kits (Model NAMC438-07) because they may be contaminated with a lubricant used during manufacturing.

    Product
    ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0118-2027·2026-10-14

    Steris HexaVue Focus Integration System Recalled for Patient Data Mismatch

    Steris is recalling 58 HexaVue Focus Integration Systems because a software issue may cause incorrect patient information to appear on printed images.

    Product
    HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and environmental control, Software Version: 2.0.18
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2027·2026-10-14

    Nihon Kohden CNS-6200 Central Nurse Station Recalled for Cybersecurity Vulnerability

    Nihon Kohden America LLC is recalling 808 CNS-6200 Series Central Nurse Stations due to a cybersecurity vulnerability that could disrupt patient monitoring.

    Product
    Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version: software versions: 01-03, 01-04, 01-05, 01-06, 02-10, 02-11, and 02-40 Product Description: The device is intended for use by medical professionals to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0115-2027·2026-10-14

    Mindray cPM Series Patient Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA, Inc. is recalling cPM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0114-2027·2026-10-14

    Mindray Recalls Passport Series Patient Monitor Operator's Manuals

    Mindray DS USA, Inc. is recalling Passport Series Patient Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0109-2027·2026-10-14

    Mindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA is recalling ePM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM 15M/ePM 10A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0113-2027·2026-10-14

    Mindray Recalls BeneView T5 and T8 Operator's Manuals for Alarm Clarification

    Mindray DS USA, Inc. is recalling 133 BeneView T5 and T8 operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    BeneView Series. Operator's Manuals: T5 / T8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0033-2027·2026-10-14

    Sun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures

    Sun Pharmaceutical Industries Inc. is recalling Tretinoin Cream USP 0.05% because the product failed impurities and degradation specifications.

    Product
    TRETINOIN — TRETINOIN (TRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0112-2027·2026-10-14

    Mindray Panorama and Telemetry Monitoring System Operator's Manuals Recalled

    Mindray DS USA, Inc. is recalling Panorama and Telemetry Monitoring System operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0110-2027·2026-10-14

    Certain Mindray patient monitor manuals need clarification of alarm functions

    Certain operator's manuals for Mindray BeneVision N1 and N-Series patient monitors contain descriptions that may be insufficient or need clarification about selected physiological alarm functions.

    Product
    BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0111-2027·2026-10-14

    Mindray BeneVision Telemetry Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA, Inc. is recalling BeneVision Series Telemetry Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0116-2027·2026-10-14

    Mindray T1 Patient Monitor Operator's Manual Recall for Alarm Descriptions

    Mindray DS USA, Inc. is recalling T1 Patient Monitor Operator's Manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    T1 Patient Monitor. Operator's Manual: T1 Patient Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V672000·2026-10-13

    KZRV SportTrek Fifth Wheel Trailers Recalled for Wiring Fire Risk

    K.Z., Inc. is recalling 2026-2027 SportTrek Fifth Wheel recreational trailers because the charge line may lack circuit protection, increasing the risk of a fire.

    Product
    KZRV — KZRV SPORTTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V671000·2026-10-09

    Volvo Recalls EX30 and EX30CC Vehicles for Head Restraint Defect

    Volvo is recalling 2025-2026 EX30 and 2026 EX30CC vehicles because the head restraint cushion may detach during a crash, increasing injury risk.

    Product
    VOLVO — 2025 VOLVO EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V663000·2026-10-09

    Honda Recalls Hybrid and Fuel Cell Vehicles for Tire Repair Kit Defect

    Honda is recalling 2023-2026 CR-V Hybrid, Accord Hybrid, and 2025 CR-V Fuel Cell EV vehicles because the tire repair kit bottle cap may detach and become a projectile.

    Product
    HONDA — 2024 HONDA ACCORD HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide