State

North Dakota product recalls

72,940 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total: 2,921
Critical: 265
Severe: 727
Most recent: 2026-09-02

Of the 2,921 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 727 (25%) are Severe.

Which agencies issued them

These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4876–4900 of 75861

CriticalFDA (Devices)·Z-0035-2026·2025-10-15
Infusion pump sets recalled over flow rate and occlusion alarm accuracy
CareFusion is recalling BD Alaris Pump Infusion Sets because the pump module used with them may perform outside established ranges for flow rate, bolus accuracy and occlusion alarm timing.
Product
BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10015414, 180 Micron Filter 2447-0007, Ball Valve SmartSite Port (Burette) 2 SmartSites Y-Sites 24201-0007, 2 SmartSite Y-sites
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0069-2026·2025-10-15
Heart pump controllers recalled over potential operating system cybersecurity vulnerabilities
Abiomed is recalling 10,153 Automated Impella Controllers over potential cybersecurity vulnerabilities related to the controller's operating system.
Product
Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V703000·2025-10-15
International Recalls 2026 IC Bus CESB School Buses for Transmission Defect
International is recalling 2026 IC Bus CESB school buses because a transmission shift actuator may not be calibrated properly, preventing reverse gear engagement.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V700000·2025-10-15
BMW Recalls 2018 328D Models Due to EGR Cooler Fire Risk
BMW is recalling 2018 328D diesel vehicles because a leaking EGR cooler can cause smoldering particles and a melting intake manifold, increasing the risk of a fire.
Product
BMW — BMW 328D
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0056-2026·2025-10-15
L-Arginine HCl injection recalled across all lots over sterility assurance
GenoGenix is recalling L-Arginine HCl for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
L-Arginine HCl for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0065-2026·2025-10-15
NAD+ injection recalled across all lots for lack of sterility assurance
GenoGenix is recalling NAD+ injection at 50 mg/mL and 100 mg/mL in 10 mL multi-dose vials, covering all lots within expiry, for lack of assurance of sterility.
Product
NAD+ (Nicotinamide adenine dinucleotide), a) 50 mg/mL, b) 100 mg/mL, 10 mL multi-dose vials, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0005-2026·2025-10-15
Isopropyl hand sanitizer recalled because methanol risk could not be excluded
Acuity Specialty Products is recalling AFCO isopropyl alcohol-based hand sanitizer because required receipt testing of incoming alcohol was not performed, so methanol risk could not be excluded.
Product
AFCO, Hand Sanitizer (Isopropyl Alcohol-Based, Product 5515), Manufactured by: AFCO, 550 Development Avenue, Chambersburg, PA 17201, Toll Free: 800-345-1329, Package Configuration: a) 4x1 Gallon Case, 5 Gallon Pail, 55 Gallon Drum.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0061-2026·2025-10-15
Lysine for injection recalled across all lots over sterility assurance
GenoGenix is recalling Lysine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Lysine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2026·2025-10-15
Glycine for injection recalled across all lots over sterility assurance
GenoGenix is recalling Glycine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Glycine for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0078-2026·2025-10-15
Pentosan for injection recalled across all lots over sterility assurance
GenoGenix is recalling Pentosan for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Pentosan for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0068-2026·2025-10-15
Medical imaging servers recalled over security vulnerability affecting patient data
GE is recalling 7,302 AW Server systems after identifying a security vulnerability that, if exploited, could compromise the confidentiality, integrity and availability of patient data.
Product
AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0041-2026·2025-10-15
Preserved ascorbic acid injection recalled across all lots over sterility assurance
GenoGenix is recalling preserved Ascorbic Acid (Vitamin C) for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Ascorbic Acid (Vitamin C) for Injection, Preserved, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0003-2026·2025-10-15
Bevacizumab intravitreal syringes recalled for lack of sterility assurance
RC Outsourcing is recalling 2,669 prefilled Bevacizumab 1.75 mg/0.07 mL intravitreal syringes for lack of assurance of sterility.
Product
Bevacizumab 1.75 mg/0.07 mL - 0.25 mL syringe, Intravitreal, 0.07 mL Total Volume, Rx Only, Hospital/Office Use Only, Refrigerate, RC Outsourcing LLC, Lowellville, OH 44436.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0084-2026·2025-10-15
Zinc chloride injection recalled across all lots for lack of sterility
GenoGenix is recalling Zinc Chloride for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Zinc Chloride for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0009-2026·2025-10-15
Chlorpromazine 25 mg fifty count packs recalled over nitrosamine impurity
Major Pharmaceuticals is recalling 2,064 fifty-tablet blister packs of Chlorpromazine Hydrochloride Tablets USP 25 mg because a nitrosamine impurity exceeded the recommended intake limit.
Product
Major ChlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 50 Tablets (5x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7130-06, UPC (01)00309047130061
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0073-2026·2025-10-15
EDTA for injection recalled across all lots over sterility assurance
GenoGenix is recalling EDTA for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
EDTA for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0072-2026·2025-10-15
CoQ10 for injection recalled across all lots over sterility assurance
GenoGenix is recalling CoQ10 for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
CoQ10 for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0062-2026·2025-10-15
Magnesium chloride injection recalled across all lots over sterility assurance
GenoGenix is recalling Magnesium Chloride for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Magnesium Chloride for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0038-2026·2025-10-15
Alpha lipoic acid injection recalled across all lots over sterility assurance
GenoGenix is recalling Alpha Lipoic Acid for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Alpha Lipoic Acid for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0066-2026·2025-10-15
Taurine for injection recalled across all lots over sterility assurance
GenoGenix is recalling Taurine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Taurine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0064-2026·2025-10-15
N-Acetyl-L-Cysteine injection recalled across all lots over sterility assurance
GenoGenix is recalling N-Acetyl-L-Cysteine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
N-Acetyl-L-Cysteine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0039-2026·2025-10-15
Amino blend for injection recalled across all lots over sterility assurance
GenoGenix is recalling Amino Blend for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Amino Blend for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0047-2026·2025-10-15
B-Complex injection recalled across all lots over lack of sterility assurance
GenoGenix is recalling B-Complex for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
B-Complex for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. B-Complex with B12 also labeled as manufactured for Synergy Wellness.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0059-2026·2025-10-15
Lipo MIC with L-Carnitine injection recalled over lack of sterility assurance
GenoGenix is recalling Lipo MIC + L-Carnitine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Lipo MIC + L-Carnitine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0011-2026·2025-10-15
Chlorpromazine 50 mg tablets recalled over nitrosamine above recommended intake limit
Major Pharmaceuticals is recalling 506 blister packs of Chlorpromazine Hydrochloride Tablets USP 50 mg because N-Nitroso Desmethyl Chlorpromazine was present above the recommended intake limit.
Product
Major ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 Tablets, (10x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7131-61, UPC (01)00309047131617
Category
Drug
Distribution
Distributed nationwide