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.

26526–26550 of 78053

  • SevereFDA (Devices)·Z-1282-2021·2021-03-31

    Hitachi Arietta 850 Ultrasound System Recalled for Acoustic Output Error

    Hitachi Medical Systems America Inc. is recalling Arietta 850 ultrasound systems with specific software versions due to an error that can cause acoustic output to exceed regulatory limits.

    Product
    Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer, etc.) for the diagnostic ultrasound evaluation of Fetal, Abdominal, Intra-operative (Spec.), Intraoperative (Neuro.), Laparoscopic, Pediatric, Small Organ…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1296-2021·2021-03-31

    Getinge Operating Table System Recalled for Hydraulic Leakage Risk

    Getinge Group Logistics America, LLC is recalling 4,288 Operating Table Systems due to a potential hydraulic leakage that could cause unintended table movement.

    Product
    Operating Table System
    Category
    Medical Device
    Distribution
    41 states
  • HighNHTSA·21V225000·2021-03-31

    Harley-Davidson motorcycles recalled for faulty headlight bulbs and visibility loss

    Harley-Davidson is recalling 2019-2021 Sportster motorcycles and replacement headlight assemblies because the glass bulb may fail, causing loss of both high and low beams and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XL1200NS, XL1200C, XL883N, XL883L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V224000·2021-03-31

    2021 Porsche Macan recalled for loose shock absorber screw connections

    Certain 2021 Porsche Macan models have improperly tightened screw connections on shock absorbers, which could compromise braking and vehicle control. Porsche will repair the connections free of charge.

    Product
    PORSCHE — PORSCHE MACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1297-2021·2021-03-31

    Stryker S-Series Equipment Management System Recall for Brake Disengagement Risk

    Stryker is recalling S-Series Equipment Management Systems because capacitive touch controls may disengage when electrocautery devices are in use.

    Product
    S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected within the S-Series Finished Good Model Number o P38198 - ASM, MFR CONTROLLER, FIXED STANDARD o P38199 - ASM, MFR CONTROLLER, LIFT STANDARD o P40553 - ASM, MFR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1292-2021·2021-03-31

    Olympus Recalls TJF-Q190V Duodenoscopes Due to Reported Mucosal Injury

    Olympus is recalling 1,564 TJF-Q190V duodenoscopes and accessories worldwide due to complaints of mucosal injury associated with the forceps elevator region.

    Product
    Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source, documentation equipment, monitor, Endo Therapy accessories (such as biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2021·2021-03-31

    RayCare 3B Oncology Software Recalled for Data Loss During Upgrade

    RaySearch Laboratories AB is recalling RayCare 3B software because patient messages may be lost when upgrading from RayCare 2.

    Product
    RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information system that supports healthcare professionals in delivering cancer care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2021·2021-03-31

    Teleflex Recalls Rusch Polaris Laryngoscopes Due to Handle Cracking

    Teleflex is voluntarily recalling Rusch Polaris laryngoscopes because customers reported that the handles develop cracks or break at the hinge.

    Product
    RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1298-2021·2021-03-31

    Teleflex Recalls PLEUR-EVAC Thoracic Catheters Due to Sterility Concerns

    Teleflex is recalling 520 PLEUR-EVAC Thoracic Catheters because the company cannot guarantee the devices are sterile.

    Product
    PLEUR-EVAC Thoracic Catheters (CATHETER, IRRIGATION). The thoracic catheter is a sterile, non pyrogenic, single use device that allows drainage from the mediastinum and/or the pleural space. The thoracic catheter is composed of Phthalate-free PVC material and is available in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1278-2021·2021-03-31

    Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability

    Baxter Healthcare is recalling 1,225 Prismaflex Control Units used for Continuous Renal Replacement Therapy because tubing performance variability may cause alarms during or after system self-tests.

    Product
    Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1289-2021·2021-03-31

    Bard Marquee Biopsy Instruments Recalled for Detaching Switch

    Bard Peripheral Vascular Inc is recalling Marquee Disposable Core Biopsy Instruments because the penetration depth switch may detach during use.

    Product
    BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the "X's refer to Tyvek Lid Label.pdf" uploaded in Associated Documents
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1299-2021·2021-03-31

    Meridian ImmunoCard Mycoplasma EIA Recalled for Potential False-Negative Results

    Meridian Bioscience is recalling 8 ImmunoCard Mycoplasma EIA kits due to incorrect storage that could cause false-negative or invalid results, potentially delaying appropriate patient treatment.

    Product
    The ImmunoCard Mycoplasma EIA detects the presence of IgM to M. pneumoniae in serum - Product Usage: intended to aid in the diagnosis of recent Mycoplasma pneumoniae infection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1293-2021·2021-03-31

    Mizuho Operating Table Hand Control Units Recalled for Sliding Risk

    Mizuho OSI is recalling 26 operating table hand control units because they may cause the tabletop to slide in the opposite direction, potentially delaying surgical procedures.

    Product
    Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: intended to support a patient during surgical operations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2021·2021-03-31

    In2Bones Shannon Percutaneous Burr Recalled for Potential Breakage During Use

    In2Bones is recalling 60 units of Shannon Percutaneous Burrs due to manufacturing non-conformity that may cause the burr to break during surgery.

    Product
    In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1290-2021·2021-03-31

    Corin Trinity Hip Prosthesis Heads Recalled for Incorrect Size Labeling

    Corin Ltd is recalling 23 units of Trinity Biolox Delta Ceramic Heads due to incorrect size labeling on packaging and patient stickers.

    Product
    Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1304-2021·2021-03-31

    Cardinal Health Recalls Femoral Angiography Drapes Due to Sticking Defect

    Cardinal Health is recalling non-sterile femoral angiography drapes because a manufacturing defect causes them to stick, preventing proper application.

    Product
    Femoral Angiography Drape Bulk Non-Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1300-2021·2021-03-31

    Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance

    Cardinal Health is recalling In-View Clear Leggings Sterile because a manufacturing variance causes the plastic film to stick, potentially preventing proper application.

    Product
    In-View Clear Leggings Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1279-2021·2021-03-31

    Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability

    Baxter Healthcare is recalling 1,650 Prismaflex Control Units used for renal replacement therapy because tubing performance variability may cause alarms during or after system self-tests.

    Product
    Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1291-2021·2021-03-31

    Corin Trinity Acetabular System Recalled for Incorrect Size Labeling

    Corin Ltd is recalling 23 units of the Trinity Acetabular System because the size indicated on the packaging and patient stickers is incorrect.

    Product
    Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1302-2021·2021-03-31

    Cardinal Health Recalls In-View Clear Leggings Due to Sticking Defect

    Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the plastic film to stick, preventing proper application.

    Product
    In-View Clear Leggings Bulk Non-Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1295-2021·2021-03-31

    Ortho-Clinical Diagnostics Recalls VITROS TIBC Calibrator Kits Due to Performance Shift

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 4 and Fe Slides because TIBC results may be approximately 80 ug/dL lower than expected.

    Product
    VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC only). Used to calibrate VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems Product Code: 1204668 Impacted Products: A. VITROS Chemistry Products TIBC Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1277-2021·2021-03-31

    Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability

    Baxter Healthcare is recalling Prismaflex Control Units because tubing variability may cause alarms during self-tests. The units are used for Continuous Renal Replacement Therapy.

    Product
    Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1288-2021·2021-03-31

    Siemens Recalls 29 Interventional Fluoroscopic X-Ray Systems for Shutdowns

    Siemens is recalling 29 interventional fluoroscopic X-ray systems because the power supply may cause the computer to shut down unexpectedly.

    Product
    Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide