State

North Dakota product recalls

73,104 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 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10876–10900 of 76028

HighFDA (Drugs)·D-0574-2024·2024-07-10
FDA recalls Dream Cream topical product due to manufacturing quality violations
Little Moon Essentials voluntarily recalls Dream Cream due to manufacturing quality control violations. No illnesses reported.
Product
Little Moon Essentials, Dream Cream (Camphor 0.45%, Menthol 5%), Packaged as a) 2OZ (57G) glass jar, UPC Code 6 73673 88214 5, NDC 70722-232-02; b) 4OZ (113G) glass jar, UPC Code 6 73673 88804 8, NDC 70722-232-04; Little Moon Essentials LLC Dania Beach, Fl 33004
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2237-2024·2024-07-10
Beckman Coulter DxI 9000 Analyzer Tubing Malfunction Causes Test Errors
Beckman Coulter DxI 9000 immunoassay analyzers may produce false or delayed test results due to pneumatic tubing disconnection during operation. Nine instruments are affected across the US and Europe.
Product
Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete photometric chemistry analyzer for clinical use. It is an in-vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2224-2024·2024-07-10
Medline surgical convenience kits recalled for weak seal defects
Medline Industries is recalling 12,588 sterile surgical convenience kits due to weak seals on Pure Pouch components that may breach sterility. Products were distributed nationwide across 23 states.
Product
Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile. b. Medline Angiography Pack, Pack #DYNJ26488W, containing a Pure Pouch with…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2258-2024·2024-07-10
Prucka 3 Amplifier capacitors could fail during cardiac monitoring procedures
Capacitors in Prucka 3 Amplifiers used with CardioLab and ComboLab cardiac systems could fail, causing display oscillations and preventing visualization of heart electrical activity waveforms.
Product
Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX hemodynamic and electrophysiology recording system; and Field Replacement Units spare part #5875569 (Assy CLABIII AMP 128CH 100-240V 50-60HZ).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2239-2024·2024-07-10
Avalon Ultrasound Transducers Recalled for Inaccurate Fetal Heart Rate Monitoring
Philips is recalling Avalon ultrasound transducers used for monitoring fetal heart rate. The device may produce inaccurate measurements when monitoring multiple fetuses, potentially delaying detection of fetal distress.
Product
Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart and externally monitors fetal heart rate.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2166-2024·2024-07-10
HORIBA Fluorolog-QM Fluorescence Instrument Laser Safety Defect Recall
HORIBA recalled 4 Fluorolog-QM fluorescence instruments due to a laser safety defect. A plastic cap instead of a proper beam stop may allow a Class 4 laser beam to exit the protective enclosure.
Product
HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2231-2024·2024-07-10
Medline surgical convenience kits recalled due to weak Pure Pouch seals
Medline is recalling over 7,600 Open Heart surgical convenience kits nationwide due to weak seals on the Pure Pouch component. The seals may fail and compromise the sterility of the surgical instruments inside.
Product
Non-sterile convenience kits: Medline Open Heart CDS, Pack #CDS981759C, containing a Pure Pouch with component Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2230-2024·2024-07-10
Medline surgical convenience kits recalled for weak seal integrity
Medline surgical convenience kits containing Pure Pouch components with weak seals may fail to maintain sterility, potentially compromising the safety of contained medical instruments. Affected kits were distributed nationwide across 23 states.
Product
Non-sterile convenience kits: a. Medline Difficult Airway Tray W/O Cook, Pack #ACC010578, containing a Pure Pouch with component Reorder #DYNJ040408, Kelly Forceps/STD STR Sterile. b. Medline Adult/Child Intubation Kit, Pack #ACC010616 and Pack #ACC010616H, containing a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2242-2024·2024-07-10
ARTIS Angiography Systems Recalled for Potential Radiation Overdose
Siemens ARTIS icono angiography systems with specific detector configurations may deliver higher radiation doses than intended in rare cases. The issue occurs during the first X-ray exposure after patient registration.
Product
ARTIS is a family of dedicated angiography systems 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
HighFDA (Devices)·Z-2259-2024·2024-07-10
Stryker Flyte Hood Protective Covers Recalled Due to Expired Products
Stryker Corporation recalled Non-Sterile Flyte hood protective covers that were distributed expired. The affected medical device units may not function as intended.
Product
The Non-Sterile Flyte hood covers the user s head and neck region and is intended to be worn with commercially available gowns. The hood is donned after the Flyte helmet and before the gown, such that the hood is securely tucked inside the gown. The hood attaches to and covers…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2246-2024·2024-07-10
Portable X-Ray Cart Positioning Arm Bolt May Come Loose and Fall
First Source Inc is recalling the First Source Vision M portable X-ray cart because the bolt securing the positioning arm to the gas spring may come loose and fall onto a patient.
Product
First Source Vision M. Portable cart and platform that supports an X-ray system and laptop computer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2266-2024·2024-07-10
VITROS Chemistry FS Diluent Pack 3 Recalled for Negatively Biased Test Results
Ortho-Clinical Diagnostics is recalling VITROS Chemistry FS Diluent Pack 3, Lot 01-1645, because it may produce negatively biased results when used with CRP slides, potentially affecting patient diagnosis and care.
Product
VITROS Chemistry Products FS Diluent Pack 3, Model/Catalog Number: 6801754. Product Description: VITROS Chemistry Products FS Diluent Pack 3 comes with 3 packs per sales unit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0582-2024·2024-07-10
Sun Pharmaceutical Recalls Decitabine Injection for Microbial Contamination
Sun Pharmaceutical is recalling Decitabine for Injection (lot HAD2964A, 2,088 vials) for a Current Good Manufacturing Practice deviation. The Total Aerobic Microbial Count test on unfiltered bulk was out of specification; the product was distributed nationwide.
Product
Decitabine for Injection 50mg per vial, For intravenous infusion only Cytotoxic Agent, Sterile, Rx Only, Single-Dose Vial, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0570-2024·2024-07-10
Budesonide USP drug ingredient recalled for glass contamination
Medisca Inc. is recalling 113 bottles of Budesonide, USP (Micronized) 500 mg due to glass particulate matter contamination caused by manufacturing deviations. The product was distributed nationwide in the USA and Canada.
Product
Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2267-2024·2024-07-10
Prostate Treatment Balloons Recalled Due to Fill Volume Mislabeling
Angiodynamics is recalling IsoLoc Prostate Immobilization Balloons (ISO-100, Lot 5402) for mislabeling. Devices have 100cc fill volume but are labeled as ISO-60 (60cc).
Product
IsoLoc Prostate Immobilization Treatment Balloon Device Kit, Catalog/UPN: ISO-100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2241-2024·2024-07-10
Siemens ARTIS Angiography Systems May Deliver Unintended Radiation Doses
Siemens ARTIS icono angiography systems with certain detectors may deliver higher-than-intended radiation doses in rare cases. The issue occurs when incorrect copper prefiltration is applied during initial x-ray exposure after patient registration.
Product
ARTIS is a family of dedicated angiography systems 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
HighFDA (Drugs)·D-0579-2024·2024-07-10
Methylphenidate Hydrochloride Extended-Release Tablets Recalled for Failed Dissolution
Trigen Laboratories recalls Methylphenidate Hydrochloride Extended-Release Tablets (36mg) because a batch failed dissolution specifications. Approximately 10,448 bottles were distributed nationwide.
Product
METHYLPHENIDATE HYDROCHLORIDE — METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2257-2024·2024-07-10
Nalu Neurostimulation Kits Recalled for Manufacturing Defect and Device Failure
Nalu Medical recalls 13 neurostimulation and peripheral nerve stimulation kits due to a manufacturing defect that may prevent the implantable pulse generator from functioning, stopping pain signal inhibition.
Product
Neurostimulation Kit (Ported, Dual 8, 40 cm), REF: 71005-US Peripheral Nerve Stimulation Kit (Ported, Dual 8, 40 cm), REF: 71019-US Components of the Nalu Spinal Cord Stimulation System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2234-2024·2024-07-10
Fathom Pedicle Retractor Blades Recalled for Manufacturing Defect
SeaSpine Orthopedics recalls Fathom Pedicle-Based Retractor C/C Blades due to manufacturing defects that could cause bone fracture or damage during surgery. 21 units were distributed nationwide.
Product
Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 35-55mm Model/Catalog Number: MR2102035 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2261-2024·2024-07-10
Stryker Corporation Recalls Expired Sterile Surgical Cannula Devices
Stryker Corporation has recalled expired sterile cannula devices distributed nationwide. The devices were past their expiration date, potentially compromising sterility and device safety.
Product
This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2228-2024·2024-07-10
Medline Surgical Kits Recalled for Weak Seals Compromising Sterility
Medline is recalling 12,588 sterile surgical kits with Pure Pouch components that have weak seals, potentially compromising sterility and exposing patients and surgical teams to non-sterile instruments.
Product
Sterile convenience kits: a. Medline Retrograde PK-22025203-LF, Pack #DYNJ47873K, containing a Pure Pouch containing component Sterile Curved Kelly Hemostat, Reorder #66175. b. Medline Cath Lab Pack, Pack #DYNJ56141A, containing a Pure Pouch containing component Medline…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2227-2024·2024-07-10
Medline Birthing Room Pack surgical kits recalled due to weak sterile seals
Medline is recalling approximately 12,588 sterile surgical kits used for childbirth procedures because weak seals on Pure Pouch components may fail and compromise sterility.
Product
Sterile convenience kit: Medline Birthing Room Pack, Pack #DYNJ38429D, containing a Pure Pouch component Sterile Sharp/Blunt Scissors 5.5", Reorder #65945 and containing a Pure Pouch component Sterile 5.5" Episiotomy Scissors, Reorder #67645.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2226-2024·2024-07-10
Medline Neuro IR Surgical Kit Recalled Due to Weak Seals
Medline is recalling Neuro IR surgical convenience kits due to weak seals in the Pure Pouch component that may compromise sterility. The recall affects 12,588 kits distributed nationwide.
Product
Sterile surgical convenience kit: Medline Neuro IR Pack, Pack #DYNJ56073C, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2262-2024·2024-07-10
BD Alaris System Manager Software Connectivity Issue Recalled Nationwide
A software issue in BD Alaris System Manager version 12.5.1 may prevent the PC unit from connecting to the server, potentially affecting wireless data transmission. CareFusion 303, Inc. is recalling the affected software version nationwide.
Product
BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2256-2024·2024-07-10
BD Pyxis automated dispensing cabinets with noncertified power strips
BD Pyxis automated dispensing cabinets were shipped with socket-outlet power strips that lack IEC electrical certification, potentially exposing users to leakage currents and electric shock.
Product
BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 169-157, BD PYXIS MB TWR MN 1FM-10HH-1FH MP/ 169-143, BD PYXIS MB TWR MN 2FH-1FM-4HH-2FM MP/ 169-145, BD PYXIS MB TWR MN 2FM-8HH-1FH MP/ 169-144, BD PYXIS MB…
Category
Medical Device
Distribution
Distributed nationwide