State

North Dakota product recalls

73,088 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total: 2,924
Critical: 265
Severe: 729
Most recent: 2026-09-23

Of the 2,924 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 729 (25%) are Severe.

Which agencies issued them

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8951–8975 of 76012

SevereFDA (Devices)·Z-0293-2025·2024-11-20
Trilogy EV300 ventilator: potential flow sensor malfunction from aerosol accumulation
Philips Respironics is recalling 34,146 Trilogy EV300 ventilators due to potential aerosol accumulation on the internal flow sensor, which could cause inaccurate ventilation measurements.
Product
Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, ND2200X15B, ES2200X15B, FR2200X14B, FX2200X15B, EU2200X15B, IA2200X15B, IT2200X21B, KR2200X15B, TR2200X15B, EE2200X15B. Intended for invasive and non-invasive venti
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0294-2025·2024-11-20
Aeris EVO Ventilator May Develop Flow Sensor Fouling from Aerosols
Philips Respironics Aeris EVO ventilators may accumulate aerosol deposits on the internal flow sensor, potentially causing inaccurate flow measurements.
Product
Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0305-2025·2024-11-20
Anesthesia workstation piston ventilator may fail before or during use
Draeger Medical is recalling Atlan A350XL anesthesia workstations due to potential piston ventilator failure that may occur before use or during mechanical ventilation.
Product
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24E099000·2024-11-20
Agility Fuel Solutions Recalls CNG Fuel Systems Due to Valve Cracks
Agility Fuel Solutions is recalling certain CNG fuel systems because manual cylinder valves may develop stress corrosion cracks, causing a natural gas leak that increases fire risk.
Product
FUEL SYSTEM, OTHER recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V876000·2024-11-20
Oliver travel trailer water heater burner brackets may loosen and misdirect flame
Oliver Travel Trailers is recalling certain 2016-2024 Elite I and Elite II trailers because the Truma water heater burner bracket may loosen, misdirecting the flame.
Product
OLIVER TRAVEL TRAILERS — OLIVER TRAVEL TRAILERS LEGACY ELITE, LEGACY ELITE II
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0446-2025·2024-11-20
Halyard EP TRAY Surgical Kits Recalled for Loose Metal Flakes
AVID Medical is recalling Halyard EP TRAY surgical convenience kits due to sponge forceps and towel clamps that may shed small metal flakes. These flakes could enter surgical sites, potentially causing local or foreign body reactions.
Product
Halyard EP TRAY - Medical convenience kits Model Number: VAST038-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0412-2025·2024-11-20
Halyard Angiography Pack Surgical Instruments Recalled Due to Loose Metal Flakes
AVID Medical is recalling Halyard angiography pack surgical instruments due to loose metal flakes that could detach and enter a patient's surgical site, potentially causing foreign body reactions.
Product
Halyard ANGIOGRAPHY PACK - Medical convenience kits Model Number: MAMC218-18
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2025·2024-11-20
MEERA CL Mobile Operating Table Control Malfunction Recall
The MEERA CL mobile operating table may experience error code 50037 that stops table movement during use, causing surgical procedure delays. Getinge recalled 342 units distributed worldwide.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment, Item Number: 720001B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0442-2025·2024-11-20
Halyard Pacemaker Instrument Packs Recalled for Loose Metal Flakes
AVID Medical is recalling Halyard Pacemaker Instrument Packs (Model VAPX040-01) because sponge forceps and towel clamps may contain loose metal flakes that could detach and enter a patient's surgical site during procedures.
Product
Halyard PACEMAKER INSTRUMENT PACK - Medical convenience kits Model Number: VAPX040-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0424-2025·2024-11-20
Halyard Vaginal Gyn Pack Recalled Due to Loose Metal Flakes Risk
AVID Medical is recalling the Halyard MAJOR VAGINAL GYN PACK due to sponge forceps and towel clamps that may shed loose metal flakes. These flakes could enter a surgical site undetected, causing local reactions or foreign body reactions.
Product
Halyard MAJOR VAGINAL GYN PACK - Medical convenience kits Model Number: SAMM021-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0395-2025·2024-11-20
Halyard Total Knee Medical Kits Recalled for Potential Metal Flakes in Surgical Instruments
AVID Medical is recalling Halyard KIT, TOTAL KNEE medical convenience kits due to loose metal flakes in sponge forceps and towel clamps that could contaminate surgical sites.
Product
Halyard KIT, TOTAL KNEE - Medical convenience kits Model Number: EUOR002-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0329-2025·2024-11-20
SafeControl Bed Handset May Move Unexpectedly After Power Restoration
The SafeControl handset component of Sentida beds may revert to an active mode after power restoration, potentially causing unintended bed movement. Consumers should ensure beds are safely positioned before power interruptions.
Product
SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2025·2024-11-20
Halyard Angio Tray surgical kits recalled for loose metal flakes
AVID Medical recalls Halyard ANGIO TRAY (Model VAPX021-05) surgical kits due to potential loose metal flakes on forceps and clamps that could enter surgical sites and cause local or foreign body reactions.
Product
Halyard ANGIO TRAY - Medical convenience kits Model Number: VAPX021-05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0407-2025·2024-11-20
Surgical instrument bundle recalled for potentially detachable metal flakes
AVID Medical is recalling Halyard VAG hysterectomy instrument bundles due to loose metal flakes on surgical instruments that could contaminate surgical sites.
Product
Halyard VAG HYSTERECTOMY BUNDLE PK - Medical convenience kits Model Number: LANC022-29
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0452-2025·2024-11-20
Halyard PACK MINOR surgical instrument kits recalled for metal flake contamination
AVID Medical is recalling Halyard PACK MINOR surgical kits due to loose metal flakes that may detach from forceps and towel clamps. These flakes could potentially enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard PACK, MINOR - Medical convenience kits Model Number: VMED018-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2025·2024-11-20
Halyard Urology Laparotomy Pack surgical instruments recalled for detachable metal flakes
AVID Medical recalls Halyard Urology Laparotomy Pack surgical instruments (Model SAMM023-13, Lot 1595070) due to loose metal flakes that could detach from forceps and clamps, potentially entering surgical sites and causing foreign body reactions.
Product
Halyard UROLOGY LAPAROTOMY PACK - Medical convenience kits Model Number: SAMM023-13
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0463-2025·2024-11-20
Operating Table May Stop Unexpectedly During Surgery Due to Control Error
MEERA CL mobile operating tables may experience an error code that causes the table to stop moving unexpectedly during surgery, resulting in procedural delays.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 700001F0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0421-2025·2024-11-20
Medical Convenience Kits Recalled for Detachable Metal Flakes in Surgical Instruments
AVID Medical is recalling Halyard Shoulder Pack medical convenience kits because the sponge forceps and towel clamps contain loose metal flakes that could detach and enter a patient's surgical site during use, potentially causing foreign body reactions.
Product
Halyard SHOULDER PACK - Medical convenience kits Model Number: PANJ005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0356-2025·2024-11-20
UA Kit Specimen Containers Identified as Non-Sterile Despite Sterile Labeling
MEDLINE's UA Kit specimen containers are labeled as sterile but have been identified as non-sterile, posing a risk of contaminated specimens that could lead to incorrect test results and unnecessary treatment.
Product
UA KIT, SKU DYKM1690A; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0360-2025·2024-11-20
Urine kit specimen containers recalled for non-sterile condition
Medline urine kit specimen containers labeled as sterile are actually non-sterile. This risks sample contamination, infection, and unnecessary treatment.
Product
URINE KIT, SKU DYKM1845; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0384-2025·2024-11-20
Halyard IR Biopsy Pack recalled for loose metal flakes in surgical kit
AVID Medical is recalling Halyard IR BIOPSY PACK due to loose metal flakes in forceps and towel clamps that could detach and enter the surgical site, potentially causing local or foreign body reactions.
Product
Halyard IR BIOPSY PACK - Medical convenience kits Model Number: AVMD019-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0440-2025·2024-11-20
Halyard Biopsy Pack surgical instruments recalled due to loose metal flakes
AVID Medical is recalling Halyard BIOPSY PACK surgical kits due to loose metal flakes from sponge forceps and towel clamps. Metal flakes could enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard BIOPSY PACK - Medical convenience kits Model Number: VANW019-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0355-2025·2024-11-20
Medical Laboratory Kit Recalled Due to Non-Sterile Specimen Container
Medline Industries is recalling over 626,000 laboratory kits because the included specimen container is labeled as sterile but is actually non-sterile. Non-sterile containers risk sample contamination and may result in unnecessary treatment or prolonged hospitalization.
Product
Lab Kit, SKU DYLAB1018; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0370-2025·2024-11-20
Stryker Smoke Evacuation Pencils Recalled for Unintended Activation Risk
Stryker is recalling 403,730 Neptune SafeAir Smoke Evacuation Pencil units because they may activate unexpectedly when plugged in, creating a risk of electrical burns to patients and physicians.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button, Bulk Non-sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuatio
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0415-2025·2024-11-20
Halyard ORTHO PACK surgical instrument kits recalled due to metal flakes
AVID Medical is recalling Halyard ORTHO PACK kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard ORTHO PACK -Medical convenience kits Model Number: MMOK006-04
Category
Medical Device
Distribution
Distributed nationwide