# FDA recall Z-2926-2018

> **Stanbio Laboratory, LP** · Class II · device recall initiated 2018-02-08.

## Product

Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series.  The firm name on the label for the HemoPoint H2 shows Manufactured by EKF-diagnostic GmbH, Germany.

## Reason for recall

The US prong (type A) adapter plate may crack, break, or detach and remain in the electrical outlet exposing live electrical contacts.

## Distribution

Distribution was nationwide.  There was military distribution and no government distribution.  Foreign distribution was made to Bolivia, Malaysia, Mexico, Papua New Guinea, Paraguay, Philippines, and Suriname.

## Key facts

- **Recall number:** Z-2926-2018
- **Recalling firm:** Stanbio Laboratory, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-08
- **Report date:** 2018-09-05
- **Termination date:** 2020-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Boerne, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2926-2018

## Citation

> AI Analytics. FDA recall Z-2926-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2926-2018. Source: US FDA. Licensed CC0.

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