Nova Biomedical StatStrip Glucose Hospital Meter recalled over See official notice
What to do
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Confirm the details against the official FDA notice before acting.
Does this affect you?
Check the product in your home against the recalled item:
- Product as filed
- Nova Biomedical® — Global Medical Device Correction for StatStrip® Glucose Hospital Meter
Full recall details
- Reason for recall
- WALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. When a patient ID barcode is scanned, pri
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- Nova Biomedical®
- Recall type
- Voluntary
- Quantity
- Distribution
- While working on resolution to the patient ID issue, Nova is providing the following recommendations to end users: To mitigate the risk of glucose results being assigned to the wrong patient’s medical record, Nova recommends the use of patient validation and operator log o software configurations available in current Statstrip Glucose Hospital meter system and NovaNet middleware.
Frequently asked questions
Is Nova Biomedical StatStrip Glucose Hospital Meter recalled?
Yes. It was recalled on October 5, 2026 because wALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. When a patient ID barcode is scanned, pri.
What should I do if I have it?
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Which states are affected?
Affected states: ID.
How do I identify the recalled product?
The notice lists no UPC or lot code. Match the brand, product name and package size against the official FDA notice.
How serious is a Class II recall?
Class II means possible temporary or reversible harm.
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