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Recall Observatory FDA recall evidence

Device product

DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361

Z-0921-2025

October 07, 2024

Class II

Product summary

Firm
DRG International, Inc.
Event
Event 95785
Status
Ongoing
Classification
Class II
Quantity
10 units
Official record key
device-enforcement:Z-0921-2025

Official wording

Reason: The user of the assay may either face a failure message during re-calibration of the Hybrid.XL instrument using the re-calibration R1 and R2 of the device or find controls out of specification (failed Control High) which causes a delay in results.

Code information: UDI: (01)04048474053616(17)20251130(10)429K084-1. Lot Number: 429K084-1

Distribution pattern: Worldwide - US Nationwide distribution in the state of New Jersey and the countries of Czechia and Romania.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out of specification