State

North Dakota product recalls

72,820 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 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

526–550 of 75741

HighFDA (Devices)·Z-2783-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. PROSTATE ROBOTIC DYNJ901822B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0727-2026·2026-07-29
Naropin Injection Recall Over Particulate Matter Contamination
Fresenius Kabi is recalling 92,600 vials of NAROPIN (ropivacaine hydrochloride) injection, 0.5%, 10/2028, due to the presence of particulate matter, including hair, found in the product.
Product
NAROPIN — NAROPIN (ROPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0710-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (125 mcg) because the medication may be subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2787-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0709-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns
Major Pharmaceuticals is voluntarily recalling certain lots of Levothyroxine Sodium Tablets (75 mcg) because the medication may be subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0701-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled for Subpotency by Major Pharmaceuticals
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (50 mcg) from lot N02200 due to subpotency, meaning the tablets may contain less active ingredient than labeled. Products were distributed nationwide in the USA.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26E050000·2026-07-29
Toyota Recalls Side Curtain Air Bag Assemblies for Tacoma Vehicles
Toyota is recalling side curtain air bag assemblies for 2016-2023 Tacoma vehicles because they may be improperly secured, increasing injury risk during a crash.
Product
AIR BAGS:SIDE/WINDOW:CURTAIN recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0721-2026·2026-07-29
ROHTO DRY-AID Eye Drops Recalled Due to Sterility Concerns
The FDA is recalling ROHTO DRY-AID cooling eye drops due to lack of assurance of sterility. The product was distributed nationwide in the United States.
Product
Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, TWIN PACK 0.34 FL OZ (10 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011159, NDC 10742-8162-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2755-2026·2026-07-29
FARADRIVE STEERABLE SHEATH CLEAR Medical Device Recall
Boston Scientific recalls FARADRIVE STEERABLE SHEATH CLEAR due to valve damage risk that could cause air embolism during heart procedures.
Product
FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, IFU Reference Number LBL1062
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0728-2026·2026-07-29
Xylocaine Injection Recall Due to Hair Contamination
Fresenius Kabi is recalling 93,250 vials of Xylocaine (lidocaine HCl) injection due to the presence of particulate matter, specifically hair found in the product.
Product
XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2757-2026·2026-07-29
Boston Scientific Steerable Sheath Recall Over Hemostatic Valve Damage
Boston Scientific is recalling its Faradrive Steerable Sheath devices due to potential hemostatic valve damage during preparation, which may cause air ingress and patient harm.
Product
FARADRIVE STEERABLE SHEATH CLEAR OUS, used to facilitate access to the vasculature and into the chambers of the heart, Material Number M004PFCE21M402, IFU Reference Number 51659727-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2780-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. DAVINCI PROSTATE PACK DYNJ68477L DYNJ68477M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2786-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. SM-LAPAROSCOPIC PROSTATE PAC DYNJ61206J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2785-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. RR-DAVINCI PROSTATE ACCESSORY DYNJ63392F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2782-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. NON MB DAVINCI LITHOTOMY SM PK DYNJT6105
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0722-2026·2026-07-29
Rohto Cooling Eye Drops Recalled Due to Lack of Assurance of Sterility
Rohto-Mentholatum (Vietnam) Co., Ltd. is recalling certain lots of Rohto Cooling Eye Drops because the company cannot assure the sterility of the product.
Product
ROHTO — ROHTO (NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2781-2026·2026-07-29
Medline Urology Robotic Procedure Packs Recalled Due to Catheter Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. UROLOGY ROBOTIC PROCEDURE PACK DYNJ0945779U
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2768-2026·2026-07-29
Medtronic Neurosurgery Recalls Ventriculostomy Kit Due to High Endotoxin Levels
Medtronic Neurosurgery is recalling Ventriculostomy Kit (REF: 46154) because endotoxin levels may exceed acceptable limits for devices contacting cerebrospinal fluid.
Product
Ventriculostomy Kit, REF: 46154
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2754-2026·2026-07-29
FARADRIVE Steerable Sheath Clear IDE Recall for Air Embolism Risk
Boston Scientific recalls 400 units of a cardiac catheter sheath due to potential air embolism risk from valve damage during preparation.
Product
FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21C602, IFU Reference Number 51636751-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2778-2026·2026-07-29
MiniMed Go App Recalled Due to Missed Insulin Alerts
Medtronic is recalling its MiniMed Go app because a software bug can prevent insulin dose alerts during nighttime, potentially leading to missed doses and hyperglycemia.
Product
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0724-2026·2026-07-29
Cyproheptadine Hydrochloride Syrup Recall Due to Precipitate
Rising Pharma is recalling cyproheptadine hydrochloride syrup due to the presence of precipitate, including crystallization and floating particles in the bottle.
Product
CYPROHEPTADINE HYDROCHLORIDE — CYPROHEPTADINE HYDROCHLORIDE (CYPROHEPTADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2773-2026·2026-07-29
Pipeline Flex Embolization Devices Recalled Due to Incorrect Labeling of Implant Length
Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labeled implant length does not match the actual device length.
Product
Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. Intracranial aneurysm flow diverter
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2769-2026·2026-07-29
Silent Nite Sleep Appliance Recalled Due to Lack of FDA Clearance
Prismatik Dentalcraft, Inc. is recalling Silent Nite Sleep Appliances because the device does not have FDA clearance.
Product
Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description: Silent Nite Sleep Appliance is a mandibular advancement device (MAD) intended to treat snoring and mild to moderate obstructive sleep apnea (OSA).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2763-2026·2026-07-29
Halyard EYE PACK Convenience Kits Recalled Due to Incorrect Betadine Concentration
AVID Medical, Inc. is recalling certain Halyard EYE PACK convenience kits because the Betadine solution contained within them has an incorrect concentration.
Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2761-2026·2026-07-29
Olympus 4K UHD LCD Monitors Recalled Due to Potential Connector Faults
Olympus Corporation of the Americas is recalling 10 Olympus 4K UHD LCD Monitors (Model OEV321UH) because the HDMI and DisplayPort connectors may become faulty.
Product
Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.
Category
Medical Device
Distribution
Distributed nationwide