The Recall Desk

State

New Hampshire product recalls

73,718 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,482
Critical
603
Severe
1,048
Most recent
2026-10-28

Of the 4,482 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 1,048 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29426–29450 of 78200

  • HighFDA (Devices)·Z-2640-2020·2020-07-29

    EHOB Expansion Control Overlay Recalled for Potential Blood Contamination

    EHOB, Inc. is recalling 173 Expansion Control Overlays (Item No. 1004EC) because a portion of the lot may have been contaminated with blood.

    Product
    Expansion Control Overlay, Item No. 1004EC - Product Usage: The EHOB WAFFLE Overlay is more than a support surface, assisting in lateral transfers, boosts and turns to protect patients throughout the hospital journey. Through immersion and envelopment, the WAFFLE Overlay is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2656-2020·2020-07-29

    Carefusion Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Tray Recalled

    Carefusion 2200 Inc is recalling Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.

    Product
    Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Tray
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-2677-2020·2020-07-29

    Boston Scientific Recalls IceFORCE 2.1 CX Cryoablation Needles

    Boston Scientific is recalling 39 IceFORCE 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceFORCE 2.1 CX Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2683-2020·2020-07-29

    Boston Scientific Recalls IceForce 2.1 CX Cryoablation Needles

    Boston Scientific is recalling 656 IceForce 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceForce 2.1 CX 90 Cyroablation Needles, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2644-2020·2020-07-29

    Wellspect Recalls LoFric Origo Urinary Catheters Due to Tip Defect

    Wellspect HealthCare is voluntarily recalling LoFric Origo urinary catheters due to a potential defect in the distal tip.

    Product
    LoFric Origo, Tiemann, 16in, FR12 urinary catheters
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Devices)·Z-2687-2020·2020-07-29

    Sysmex PS-10 Sample Preparation System Recalled for Insufficient Antibody

    Sysmex America, Inc. is recalling eight PS-10 Sample Preparation Systems because they may contain insufficient antibody without triggering an error message or alarm.

    Product
    Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product Usage: is a fully automated, user configurable, open system intended for use to prepare human specimens for subsequent analysis on flow cytometers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2681-2020·2020-07-29

    Boston Scientific Recalls Prostate Cryoablation Kits Due to Needle Surface Deterioration

    Boston Scientific is recalling 71 IceFORCE 2.1 Prostate Cryoablation Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, Three IceFORCE 2.1 Prostate Cyroablation Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V444000·2020-07-29

    Thor Motor Coach motorhomes recalled for faulty swivel seat wiring harnesses

    Certain 2020-2021 Thor motorhomes with swivel seats have wiring harnesses that may be routed incorrectly, potentially causing side airbags to deploy inadvertently or fail during crashes. Owners should contact Thor or Mercedes-Benz for free inspection and repair.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH GEMINI, COMPASS, redundant SYNERGY, CHATEAU CITATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2675-2020·2020-07-29

    Boston Scientific Recalls IceFORCE Cryoablation Needles Due to Surface Deterioration

    Boston Scientific is recalling 18,440 IceFORCE 2.1 CX 90 Needle Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceFORCE 2.1 CX 90 Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2645-2020·2020-07-29

    Wellspect Recalls LoFric Origo Urethral Catheters Due to Tip Defect

    Wellspect HealthCare is voluntarily recalling specific LoFric Origo urethral catheters due to a potential defect in the distal tip.

    Product
    LoFric Origo, Tiemann, 16in, FR14 urinary catheters
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Devices)·Z-2646-2020·2020-07-29

    Carefusion Thora-Para Catheter Drainage Tray Recalled for Valve Leakage

    Carefusion 2200 Inc is recalling Thora-Para 5 Fr Non-Valved Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.

    Product
    Thora-Para 5 Fr Non-Valved Catheter Drainage Tray
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-2688-2020·2020-07-29

    Siemens syngo.via RT Image Suite Software Recall for Geometry Errors

    Siemens is recalling syngo.via RT Image Suite software versions VB30 and VB40 because modified MR image orientations may result in incorrect geometry and radiation treatment plans.

    Product
    syngo.via RT Image Suite with software versions syngo.via VB30 or VB40
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2690-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 100mm, 18G, 10mm, CS Product Number: AC0005 GTIN /UPN: 20763000153551 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2692-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recall for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe may catch on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 100mm, 20G, 10mm, CS Product Number: AC0009 GTIN / UPN: 20763000153599 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2691-2020·2020-07-29

    Medtronic Recalls Accurian RF Ablation Cannulas Due to Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probes may catch on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 150mm, 18G, 10mm, CS Product Number: AC0007 GTIN / UPN: 20763000153568 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2693-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probes catch on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2695-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation,Cannula pk, Accurian, 100mm, 22G, 10mm, SS Product Number: AC0019 GTIN / UPN: 20763000153667 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2694-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 100mm, 22G, 5mm, CS Product Number: AC0016 GTIN / UPN: 20763000153674 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2684-2020·2020-07-29

    Nuvasive NVM5 EMG Module Recalled for Incorrect Component

    NuVasive Inc is recalling 23 NVM5 EMG Modules because they contain an incorrect SSEP harness instead of the correct NVM5 Harness, potentially delaying spinal surgery monitoring.

    Product
    Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide