# FDA recall Z-2554-2026

> **IPG Medical Corporation** · Class II · device recall initiated 2026-05-05.

## Product

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

## Reason for recall

Software anomaly that causes a false display of error code 5018.

## Distribution

US Nationwide distribution in the state of MA.

## Key facts

- **Recall number:** Z-2554-2026
- **Recalling firm:** IPG Medical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-05
- **Report date:** 2026-07-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marlborough, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2554-2026

## Citation

> MORVS. FDA recall Z-2554-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2554-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*