State

North Dakota product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7201–7225 of 75905

HighFDA (Devices)·Z-1461-2025·2025-04-02
Medline Procedure Kits Recalled for Syringe Leaks and Breakage
Medline Industries is recalling 2,161 medical procedure kits containing plastic syringes with leaks and breakage issues. The affected syringes pose a potential risk to patient health and are distributed in the US and Canada.
Product
Medline procedure kits labeled as: 1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C; 2) BLEPH/RHINO PACK, Pack Number DYNJ64669A; 3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C; 4) DENTAL PACK, Pack Number DYNJ54064; 5) EAR PACK, Pack Number DYNJ68678C; 6) EN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1463-2025·2025-04-02
Medline medical procedure kits recalled for plastic syringe defects
Medline procedure kits with plastic syringes are being recalled due to potential leaks and breakage that may affect patient safety. The recall impacts 1152 units distributed nationwide and in Canada.
Product
Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1448-2025·2025-04-02
Medline C-section procedure kits recalled for syringe quality defects
Medline is recalling C-section procedure kits because plastic syringes in the kits may leak or break. The defect was identified in connection with an FDA safety alert and poses a potential risk to patient health.
Product
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ57622; 2) C SECTION PACK, Pack Number DYNJ48483B; 3) C SECTION PACK, Pack Number DYNJ61573; 4) C SECTION PACK, Pack Number DYNJ66801; 5) C SECTION PACK-LF, Pack Number DYNJ0367951P; 6) C SECTION PACK-LF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1450-2025·2025-04-02
Medline Medical Procedure Kits With Plastic Syringes Recalled for Quality Issues
Medline medical procedure kits containing plastic syringes are being recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health.
Product
Medline procedure kits labeled as: 1) L S GYN PACK, Pack Number DYNJ65616C; 2) MAIN CYSTO, Pack Number DYNJ61371A; 3) OB PACK-LF, Pack Number DYNJ20720C; 4) PELVISCOPY PACK-LF, Pack Number DYNJ0415776N; 5) POSTERIOR EYE PACK-LF, Pack Number PHS656483I; 6) ROBOTICS PA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1468-2025·2025-04-02
Progressa bed surfaces recalled for mattress dips when head elevated
Baxter Healthcare's Progressa Bed Surfaces may develop dips in the mattress when the head of the bed is elevated, as air bladders inside can shift out of position. This could reduce the bed's effectiveness at preventing pressure ulcers.
Product
Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2025·2025-04-02
Medline Delivery and Labor Kits Recalled for Defective Plastic Syringes
Medline is recalling 1,958 delivery and labor procedure kits containing plastic syringes with leaks, breakage, and quality defects that may pose a risk to patient health.
Product
Medline procedure kits labeled as: 1) DELIVERY PACK, Pack Number DYNJ0923016; 2) DELIVERY PACK-LF, Pack Number DYNJ0968863M; 3) L & D PACK-LF, Pack Number DYNJ0373290N; 4) L&D PACK, Pack Number DYNJ51998A; 5) LABOR & DELIVERY PACK-LF, Pack Number DYNJ0348455P; 6) LAB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1417-2025·2025-04-02
Baxter TruSystem 7500 Hybrid software issue disables upper back adjustment
Baxter TruSystem 7500 Hybrid affected by software issue that prevents the upper back section from being operable or adjustable when emergency mode is enabled. Affects 10 units distributed nationwide.
Product
Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1408-2025·2025-04-02
Premier Solo Diamond dental burs recalled due to material hardness defect
Premier Dental Products Co is recalling Premier Solo Diamond Large dental burs because the material hardness does not meet specifications and may cause the burs to bend during use. 77 units in six U.S. states are affected.
Product
Premier Solo Diamond - Large Invented Cone; SKU: 807016C.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1466-2025·2025-04-02
Checkpoint Guardian Intraoperative Lead adhesive defect electrical leakage risk
The adhesive on Checkpoint Guardian Intraoperative Leads may not fully cover metallic wire components, leading to potential electrical current leakage. This could result in inconsistent muscle responses and affect surgical effectiveness.
Product
Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Small Model/Catalog Number: REF# 9524 (Small) Product Description: The Checkpoint Guardian Intraoperative Leads are single-patient disposable accessories for providing s
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0294-2025·2025-04-02
Testosterone Gel Recalled Nationwide Due to Benzene Contamination
Strides Pharma is recalling Testosterone Gel 1% nationwide due to the presence of benzene, a toxic substance. Patients should contact their healthcare provider about alternative treatment options.
Product
TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1430-2025·2025-04-02
Pressure Monitoring Lines Recalled for Manufacturing Defect in Luer Fittings
Medline Industries is recalling namic medical convenience kits containing Pressure Monitoring Lines with defective female luer fittings manufactured with excess material. The defect could impair device function.
Product
namic convenience kits labeled as: MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG; medical convenience kit, REF 600605710
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1452-2025·2025-04-02
Medline arthroscopy procedure kits recalled for defective plastic syringes
Medline is recalling arthroscopy procedure kits containing plastic syringes with defects including leaks and breakage. The syringes may pose a risk to patient health during surgical procedures.
Product
Medline procedure kits labeled as: 1) ARTHROSCOPY PACK, Pack Number DYNJHS0101I; 2) ARTHROSCOPY PACK-LF, Pack Number DYNJ0390808F; 3) ARTHROSCOPY PACK-LF, Pack Number DYNJ23150J; 4) ARTHROSCOPY PACK-LF, Pack Number DYNJ21233O; 5) ARTHROSCOPY PACK-LF, Pack Number DYNJ21
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1438-2025·2025-04-02
Medline Surgical Procedure Kits Recalled for Defective Plastic Syringes
Medline Industries recalls 3,860 surgical procedure kits with defective plastic syringes that may leak or break during use. The affected kits are distributed in the US and Canada.
Product
Medline procedure kits labeled as: 1) AV FISTULA PACK, Pack Number DYNJ80088; 2) AV FISTULA PACK-LF, Pack Number DYNJ0131782J; 3) CABG, Pack Number DYNJ906462B; 4) CABG ACCESSORY PACK-LF, Pack Number DYNJ0261346U; 5) CARDIAC CATH PACEMAKER-LF, Pack Number DYNJ42997C;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0296-2025·2025-04-02
Compounded Fentanyl-Bupivacaine Epidural Injections Recalled for Sterility Failure
QuVa Pharma recalls compounded fentanyl-bupivacaine epidural injections due to lack of assurance of sterility. The recall affects 2,310 cassettes distributed nationwide.
Product
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0292-2025·2025-04-02
Metformin Hydrochloride Extended-Release Tablets Recalled for Foreign Tablet Contamination
A-S Medication Solutions is recalling 411 bottles of Metformin Hydrochloride Extended-Release 500mg tablets (Lot #4260340) distributed nationwide due to the presence of foreign tablets or capsules.
Product
METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1413-2025·2025-04-02
Baxter Mobile column TruSystem 7500 U emergency mode software issue affects back adjustment
A software issue in the Baxter Mobile column TruSystem 7500 U prevents the upper back section from being operable or adjustable when emergency mode is enabled. Approximately 40 units distributed nationwide are affected.
Product
Baxter Mobile column TruSystem 7500 U, Product Code 1730720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1454-2025·2025-04-02
Helix Elite Quality Control Material Recalled for Delayed Detection and QC Failure
Microbiologics Inc is recalling its Helix Elite RSV quality control material (Lot HE0044-131) because the RSV component may produce delayed test results and could fail quality control checks. This Class II recall affects 28 units distributed worldwide.
Product
Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory Syncytial Virus, Multi-analyte, unassayed quality control material, Catalog Number HE0044N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1462-2025·2025-04-02
Medline Surgical Procedure Kits Recalled for Defective Plastic Syringes
Medline Industries is recalling 1,228 surgical procedure kits containing defective plastic syringes. The syringes may leak or break during use, potentially affecting patient safety.
Product
Medline procedure kits labeled as: 1) BREAST PACK-LF, Pack Number DYNJ0956628O; 2) BREAST SURGERY FOAKS, Pack Number DYNJ63577C; 3) CHEST BREAST -LF, Pack Number DYNJCEN04C; 4) DIEP PACK, Pack Number DYNJ60669G; 5) FACE LIFT PACK, Pack Number DYNJ64670B; 6) FREE FLAP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2025·2025-04-02
Baxter surgical table software issue blocks emergency back adjustment
Baxter is recalling 112 units of the TruSystem 7500 surgical table due to a software issue preventing upper back adjustment during emergency mode. No injuries have been reported.
Product
Baxter Floor mounting column TruSystem 7500, Product Code 1717021
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0666-2025·2025-04-02
Our Family Traverse City Cherry Ground Coffee Recalled for Mislabeling
Our Family Traverse City Cherry Ground Coffee (12 oz) has been recalled due to mislabeling. A portion of production was labeled as decaffeinated when it contains regular caffeine.
Product
COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g) UPC 0 70253 11080 1 DISTRIBUTED BY THE SPARTANNASH COMPANY GRAND RAPIDS, MI 49518
Category
Food
Distribution
15 states
ModerateFDA (Devices)·Z-1412-2025·2025-04-02
Baxter Mobile Column TruSystem 7500 Software Defect Prevents Back Adjustment
Baxter Healthcare is recalling the Mobile column TruSystem 7500 due to a software issue that prevents the upper back section from being adjusted when emergency mode is enabled. Approximately 1,596 units distributed nationwide are affected.
Product
Baxter Mobile column TruSystem 7500, Product Code 1717023
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1432-2025·2025-04-02
Orthofix Pillar SA Ti Spacer System Mislabeled for Anterior Height
Orthofix is recalling Pillar SA Ti Spacer System spinal implants because the product label lists an incorrect anterior height of 10mm, while the actual device measures 10.5mm. This labeling discrepancy could affect surgical planning during implantation.
Product
Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP, 33mm W x 24mm D x 10mm H, 7 degrees; (2) REF 82-3700SP, 37mm W x 28mm D x 10mm H, 7 degrees; and (3) REF 82-4000SP, 40mm W x 32mm D x 10mm
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1433-2025·2025-04-02
NexGen LPS Flex knee prosthesis recalled for labeling inconsistency
Zimmer recalls 76 NexGen LPS Flex knee prosthesis units due to conflicting plate compatibility information on the product label.
Product
NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model Number 00-5962-042-10
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0668-2025·2025-04-02
Dried Lily Flowers Recalled Due to Undeclared Sulfites
U.S. Trading Company recalled dried lily flowers due to undeclared sulfites, which pose a risk to people with sulfite sensitivity. The recall affected 5,200 packages distributed across 32 states and was terminated July 1, 2025.
Product
DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING COMPANY Hayward, CA 94545-1130 Product of China
Category
Food
Distribution
30 states
SevereNHTSA·25V204000·2025-04-01
Bollinger Motors Recalls 2025 B4 Trucks Due to Battery Seal Defect
Bollinger Motors is recalling 2025 B4 trucks because the high-voltage battery pack may be improperly sealed, allowing liquid entry that could cause fire, shock, or loss of drive power.
Product
BOLLINGER MOTORS — BOLLINGER MOTORS B4
Category
Vehicle
Distribution
Distributed nationwide