State

North Dakota product recalls

73,566 recalls have nationwide distribution and so reach North Dakota. 2,925 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total: 2,925
Critical: 265
Severe: 869
Most recent: 2026-10-14

Of the 2,925 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 869 (30%) are Severe.

Which agencies issued them

These figures cover only the 2,925 recalls whose distribution notice names North Dakota specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24951–24975 of 76491

HighFDA (Devices)·Z-2257-2021·2021-08-18
Beckman Coulter SARS-CoV-2 Antigen QC Reagent Recalled Due to False Positive Risk
Beckman Coulter is recalling ACCESS SARS-CoV-2 Antigen QC reagent due to false positive test results that could lead to incorrect diagnoses. The Class II recall affects 544 units distributed nationally and internationally.
Product
ACCESS SARS-CoV-2 ANTIGEN QC, REF: C68670, CONTENTS: 3 X 6.0 mL QC1, 3 x 6.0 mL QC2, 1 QC VALUE CARD, IVD, Rx Only, UDI: (01)15099590742737;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2246-2021·2021-08-18
Mislabeled Cutting Electrode May Contain Wrong Electrode Type
Richard Wolf's Cutting Electrode Bipo 24.5FR may be mislabeled and contain a BIVAP electrode instead. Affected lot 21002858 was distributed to healthcare facilities in five states.
Product
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2274-2021·2021-08-18
FDA Recalls Biomet Hip Implant for Potential Fretting Corrosion
Biomet is recalling its Arcos Modular Revision Hip System Standard Cone Prox Body due to risk of fretting corrosion and device failure in the inner taper. Affected patients should consult their surgeon.
Product
Arcos Modular Revision Hip System Standard Cone Prox Body, Size C, 80 MM Item Number: 11-301343
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2255-2021·2021-08-18
Beckman Coulter SARS-CoV-2 Test Recalled for False Positive Risk
Beckman Coulter is recalling its ACCESS SARS-CoV-2 Antigen test (REF C68668) because it may produce false positive results, potentially leading to incorrect diagnoses.
Product
ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2259-2021·2021-08-18
Arcos Modular Hip Implant Cone Bodies Recalled for Fretting Corrosion
Biomet is recalling specific lots of Arcos Modular Revision Hip System cone bodies due to potential fretting corrosion and device failure that could require surgical intervention.
Product
Arcos Modular Revision Hip System Standard Cone Prox Body, Size A, 50 MM Item Number: 11-301300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2273-2021·2021-08-18
Biomet Hip Implant System Recalled Due to Potential Fretting Corrosion
Biomet is recalling the Arcos Modular Revision Hip System component due to potential inner taper fretting corrosion that could lead to device failure requiring surgery. No injuries have been reported.
Product
Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 80 MM Item Number: 11-301342
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2247-2021·2021-08-18
Jamshidi Bone Marrow Biopsy Needles Recalled for Packaging Seal Defects
Bard Peripheral Vascular Inc. is recalling multiple models of Jamshidi bone marrow biopsy needles due to incomplete or open packaging seals that may compromise sterility. No illnesses or injuries have been reported.
Product
TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513 Jamshidi" Bone Marrow Biopsy/Aspiration Needle. 13G x 8.9 cm; TJM4011 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 11G x…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0857-2021·2021-08-18
5000 Years Foods Baby Napa Kimchi Recall for Listeria Contamination
5000 Years Foods is recalling Baby Napa Kimchi in 128 oz, 64 oz, and 32 oz glass jars due to potential contamination with Listeria monocytogenes. The product was distributed in Illinois and potentially nationwide through retail distributors.
Product
5000 Years Foods BABY NAPA KIMCHI in 128 oz, 64 oz, and 32 oz glass jars
Category
Food
Distribution
Distributed nationwide
HighCPSC·21182·2021-08-18
B-Air VP-33 Blower Fans Recalled Due to Fire Hazard
Intertex is recalling about 29,500 B-Air VP-33 blower fans because the capacitor can overheat and pose a fire hazard. The firm has received five reports of fire-related property damage totaling about $75,000, though no injuries have been reported.
Product
B-Air VP-33 Blower Fans
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2223-2021·2021-08-18
Stryker GoBed II Medical Bed Recalled for Improper Home Distribution
Stryker's GoBed II MedSurg Bed was distributed to residential customers but is intended for healthcare facility use. Home users may not understand professional-level safety instructions, creating a risk of misuse.
Product
GoBed II MedSurg Bed, Model Number FL28, Part #FL28EX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0854-2021·2021-08-18
5000 Years Foods Kimchi Recalled for Listeria Contamination Risk
5000 Years Foods is recalling NO MSG JULRADO WHOLE CABBAGE KIMCHI in 128 oz and 64 oz glass jars due to potential Listeria monocytogenes contamination. The affected product was distributed through Illinois and reached customers nationwide.
Product
5000 Years Foods NO MSG JULRADO WHOLE CABBAGE KIMCHI in 128 oz and 64 oz glass jars
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0856-2021·2021-08-18
5000 Years Foods White Whole Kimchi Recall Due to Listeria Risk
5000 Years Foods is recalling White Whole Kimchi in 32 oz, 64 oz, and 128 oz glass jars due to potential Listeria monocytogenes contamination. The affected product was distributed through Illinois to retail locations potentially nationwide.
Product
5000 Years Foods WHITE WHOLE KIMCHI in 128 oz, 64 oz, and 32 oz glass jars
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0722-2021·2021-08-18
Cimetidine Hydrochloride Oral Solution Recalled for CGMP Violation
Pharmaceutical Associates Inc. is recalling Cimetidine Hydrochloride Oral Solution 300 mg/5 mL due to a lack of Current Good Manufacturing Practice (CGMP) and potential carryover of Senna Syrup.
Product
Cimetidine Hydrochloride Oral Solution 300 mg/5 mL, 8 fl oz (237 mL) Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0649-08
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2209-2021·2021-08-18
Prime TC Transport Chair Recalled for Improper Residential Distribution
The Prime TC-transport chair, designed for healthcare facility use, was distributed to residential customers who may not understand the professional-level operating instructions. The recall addresses potential risk of improper use by home users.
Product
Prime TC-transport chair intended for medical purposes to assist a person in performing an activity that the person would find difficult to do or be unable to do Model Number: 1460, Part #1460000000¿¿¿¿¿¿¿
Category
Medical Device
Distribution
Distributed nationwide
ModerateNHTSA·21V646000·2021-08-18
2022 BMW X4 Tire Information Label May Contain Incorrect Size and Pressure
BMW is recalling certain 2022 X4 vehicles because the tire information label may contain incorrect tire size and pressure information. Installing wrong-sized or improperly inflated tires increases the risk of a crash.
Product
BMW — BMW X4
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2227-2021·2021-08-18
CIRRUS HD-OCT Model 6000 imaging devices recalled for missing FDA pre-market clearance
Carl Zeiss Meditec is recalling 914 CIRRUS HD-OCT Model 6000 imaging devices. The manufacturer failed to obtain FDA pre-market clearance before selling the devices.
Product
Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
Category
Medical Device
Distribution
53 states
ModerateFDA (Devices)·Z-2215-2021·2021-08-18
Support Surface Device Distributed to Home Patients Without Healthcare Professional Instructions
An Isolibrium Support Surface intended for healthcare facilities was distributed to home customers. While the labeling is correct, home users may not understand instructions intended for healthcare professionals.
Product
Isolibrium Support Surface - support surface assists in the prevention and treatment of all pressure injury stages (including stages 1, 2, 3, 4, Unstageable and Deep Tissue Pressure Injury, Model Number: 2972, Part # 2972000000
Category
Medical Device
Distribution
Distributed nationwide
ModerateCPSC·21185·2021-08-18
Primark Recalls 8-Pack Scent Stamper Pens for Elevated Benzyl Alcohol
Primark is recalling about 9,500 8-pack Scent Stamper Pens due to elevated levels of benzyl alcohol in the purple pen, which poses a risk of skin irritation. No injuries have been reported.
Product
8-Pack Scent Stamper Pens
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2241-2021·2021-08-18
Kaluza C Flow Cytometry Software Recalled for Potential Erroneous Results
The FDA is recalling Kaluza C Flow Cytometry Software versions 1.0, 1.1.1, and 1.1.2 due to software anomalies that may generate erroneous results affecting diagnostic interpretation.
Product
Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License C10575 - Kaluza C Single User 1-year License C10576 - Kaluza C 10 User Network License C10577 - Kaluza C 5 User Network License C10578 - Kaluza C Single…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0721-2021·2021-08-18
Nystatin Oral Suspension Recalled Due to CGMP Violation
PAI Holdings is recalling Nystatin Oral Suspension nationwide due to a lack of Current Good Manufacturing Practice (CGMP) controls that could allow carryover of Senna Syrup into the product.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0723-2021·2021-08-18
Ethosuximide Oral Solution Recalled Due to Lack of CGMP Compliance
PAI Holdings is recalling Ethosuximide Oral Solution 250 mg/5 mL (Lot C9BC, expiration 31 October 2022) distributed nationwide due to potential carry-over contamination from Senna Syrup related to lack of current good manufacturing practices.
Product
ETHOSUXIMIDE — ETHOSUXIMIDE (ETHOSUXIMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2233-2021·2021-08-18
Medline Total Knee Surgical Kit Recalled for Expired Irrigation Component
Medline Industries is recalling Total Knee convenience kits that may contain an expired saline irrigation solution component. The expired component may not maintain proper sterility for surgical use.
Product
Medline Total Knee, convenience kit, REF DYNJ907129B, containing expired component NaCl 3000mL Irrigation Bag (exp. date 08/01/2020).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0719-2021·2021-08-18
Sulfamethoxazole and Trimethoprim Tablets Recalled for Metal Contamination
Aurobindo Pharma USA Inc. is recalling Sulfamethoxazole and Trimethoprim Tablets (800mg/160mg) due to potential metal contamination in the product. The recall affects approximately 3,800 bottles distributed nationwide.
Product
SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2210-2021·2021-08-18
InTouch 2131 Medical Device Recalled for Distribution to Residential Users
Stryker's InTouch 2131 medical device, intended for healthcare facilities, was distributed to residential customers. Home users may not understand healthcare-specific instructions, creating a risk of improper use.
Product
InTouch 2131-intended to support a human patient in an acute care setting, Model Number: 2131000000, Part #1460000000¿¿¿¿¿¿¿
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·21179·2021-08-17
Zen Magnets and Neoballs Magnets Recalled Due to Ingestion Hazard
Zen Magnets and Neoballs high-powered spherical magnets are being recalled because swallowing multiple magnets can cause intestinal perforation, blockage, and death. About 10 million magnets sold individually and in sets since January 2009 are affected.
Product
Zen Magnets and Neoballs Magnets
Category
Consumer Product
Distribution
Distributed nationwide