Skip to content
Use caution Medical device recall · FDA · Published July 29, 2026

Nova Biomedical StatStrip Glucose Meter Software Issue: Patient Data Mismatch Risk

Nova Biomedical recalls StatStrip Glucose and Ketone meters (model 63683) due to software error causing patient data mismatches. This may lead to incorrect glucose results being recorded for the wrong patient, risking inappropriate treatment for critically ill patients.

🇺🇸 FDA recall #Z-3130-2026Medical deviceNova Biomedical ›
✎ GovInfoNow plain-language explainer

Nova Biomedical is recalling its StatStrip Glucose and Ketone meters (model 63683) because a software issue causes patient data to be incorrectly recorded. This could lead to critical patients receiving wrong treatment if the error isn't noticed. Read more at govinfonow.com/recall/1134679-nova-biomedical-statstrip-glucose-meter-software-issue-patient-data-mismatch.

Source Summary by GovInfoNow · govinfonow.com/recall/1134679-nova-biomedical-statstrip-glucose-meter-software-issue-patient-data-mismatch · Updated October 4, 2026 · FDA enforcement record: FDA #Z-3130-2026

Cite this page

“Nova Biomedical StatStrip Glucose Meter Software Issue: Patient Data Mismatch Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/1134679-nova-biomedical-statstrip-glucose-meter-software-issue-patient-data-mismatch. Based on FDA recall #Z-3130-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3130-2026%22&limit=1).

The FDA announced on July 29, 2026, that Nova Biomedical Corporation is recalling the StatStrip Glucose and B-Ketone meter (Model No. 63683) due to a software defect. The hazard involves incorrect patient data transmission resulting from barcode scanning errors.

How to tell if you have it

  • Brand: Nova Biomedical
  • Product: StatStrip Glucose and B-Ketone meter
  • Model No: 63683
  • UDI-DI: 00385480636834
  • Software Versions: All versions 0.00.13.10 through 1.5.14.25
  • Quantity: 1,858 units

The hazard

A software synchronization issue causes the device to intermittently retain previously scanned barcodes, leading to incorrect patient glucose results being assigned to medical records. This defect affects both patient identification and quality control barcode scanning but does not impact analytical accuracy. The FDA reported no specific incidents or injuries in this record.

Context

GovInfoNow's records show Nova Biomedical Corporation has 3 other recalls on record since June 19, 2017. Other recent recalls of similar products include Medtronic CareLink Clinic Software Error May Cause Incorrect Glucose Readings (Oct. 21, 2025), GE Medical Systems ECG Systems Software Error Risks Patient Data Mix-Up (April 21, 2026), and GE Healthcare Centricity Enterprise Archive V2/V3/V4 Software Recall: Patient Data Mismatch Risk (July 31, 2026).

How to tell if you have this one

Check for the model number 63683 on your StatStrip Glucose and Ketone meter. The device was sold with software versions from 0.00.13.10 through 1.5.14.25.

  • Brand
    Nova Biomedical
  • Category
    Medical device
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Ongoing
  • Distribution
    Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Austria, Belgium, Bolivia, Brazil, Canada, Cayman Islands, Chile, Croatia, Dominican Rep., Finland, France, Germany, Ireland, Israel, Italy, Netherlands, New Zealand, South Korea, Switzerland, Thailand, Turkey, United Kingdom.
Recall numberProduct, codes & lotsQuantity
Z-3128-2026StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system.; Model No: 63685. UDI-DI: 00385480636858. Software Versions: All versions 0.00.13.10 through 1.5.14.25.20,616 units
Z-3129-2026StatStrip Glucose Hospital Meter System. Model No: 66739. Glucose test system.; Model No: 66739. UDI-DI: 0038548063685. Software Versions: All versions 0.00.13.10 through 1.5.14.25.10,941 units
Z-3130-2026StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system.; Model No: 63683. UDI-DI: 00385480636834. Software Versions: All versions 0.00.13.10 through 1.5.14.25.1,858 units
Z-3131-2026StatStrip Glucose and B- Ketone meter. Model No: 63910. Glucose test system.; Model No: 63910. UDI-DI: 00385480639101. Software Versions: All versions 0.00.13.10 through 1.5.14.25.8,939 units
Z-3132-2026StatStrip Glucose and B- Ketone meter. Model No: 66429. Glucose test system.; Model No: 66429. UDI-DI: :00385480664295. Software Versions: All versions 0.00.13.10 through 1.5.14.25.2,044 units
Based on the official FDA remedy

What to do — step by step

  1. Check Device Model

    Verify your meter's model number is 63683.

  2. Review Software Version

    Confirm your software version falls within the affected range (0.00.13.10 through 1.5.14.25).

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Austria, Belgium, Bolivia, Brazil, Canada, Cayman Islands, Chile, Croatia, Dominican Rep., Finland, France, Germany, Ireland, Israel, Italy, Netherlands, New Zealand,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 56 days after the firm started it.

1. Firm started the recall: Jul 29, 202612. FDA classified it Class I: Sep 11, 202623. Published in FDA’s Enforcement Report: Sep 23, 202634. Added to GovInfoNow: Sep 29, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest medical device recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-3130-2026 (July 29, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3130-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA