# FDA recall Z-2076-2019

> **LABORIE MEDICAL TECHNOLOGIES, CORP** · Class II · device recall initiated 2019-07-17.

## Product

U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics for assessing lower urinary tract dysfunctions

## Reason for recall

Power supply unit (PS-SBL) not correctly labeled, and insulation material used at the low voltage DC end does not meet all applicable flammability rating requirements. may lead to a potential fire hazard

## Distribution

US distribution in AZ, and PA.

## Key facts

- **Recall number:** Z-2076-2019
- **Recalling firm:** LABORIE MEDICAL TECHNOLOGIES, CORP
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-17
- **Report date:** 2019-07-31
- **Termination date:** 2023-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Williston, VT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2076-2019

## Citation

> AI Analytics. FDA recall Z-2076-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2076-2019. Source: US FDA. Licensed CC0.

---

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