International Medical Devices Database

Manufacturer Address
Hypoguard USA, Inc., 5182 W 76th St, Edina MN 55439-2900
Source
USFDA
2 Events
- Recall of Device Recall Hypoguard Advance
- Recall of Device Recall Hypoguard Advance

2 devices in the database

Device Recall Hypoguard Advance

Model / Serial
Lots 01143A, 02263A, 03103A, 10222A, 12212A, 12312A, 03183A, 04293A, and 05273A
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
The product was distributed to consignees located nationwide in the United States.
Product Description
Hypoguard Advance Blood Glucose Monitoring System, includes Hypoguard Advance Blood Glucose Meter and 10 Hypoguard Advance Blood Glucose Strips

Device Recall Hypoguard Advance

Model / Serial
01143A, 01023A, 01173A, 01293A, 01293B, 01303A 01303B, 02263A, 02263B, 02273A, 02273B, 02273C, 03113A, 11182A, 12282A, 12302A, 03113A, 03213A, 03263A, 03283A, 03283B, 04153A, 05293B, 04153B, 05293C, 04213A, 05293A, 04303A, 06063A, 05293D, and 05303A
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
The product was distributed to consignees located nationwide in the United States.
Product Description
Hypoguard Advance Blood Glucose Strips, 10, 50, and 100 strip bottles.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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Hypoguard USA, Inc.

2 devices in the database

Device Recall Hypoguard Advance

Device Recall Hypoguard Advance