# FDA recall Z-0807-2025

> **Stryker Corporation** · Class II · device recall initiated 2024-12-03.

## Product

100V NEPTUNE 3 ROVER JAPANESE (0703-003-000)  120V NEPTUNE S ROVER (0711-001-000)  230V NEPTUNE 3 ROVER ENGLISH (0703-002-000ENG)  230V NEPTUNE 3 ROVER SPANISH (0703-002-000ES)

## Reason for recall

Bolts on the vacuum pump filter housing and the flange plate were not properly tightened, impacting the function of the Neptune rovers. Systems with loose bolts may fail to provide sufficient suction force or loss of suction during a procedure.

## Distribution

US (Domestic) distribution to states of: WA, GA, and IL. OUS (International) distribution to Japan and Netherlands.

## Key facts

- **Recall number:** Z-0807-2025
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-03
- **Report date:** 2025-01-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0807-2025

## Citation

> AI Analytics. FDA recall Z-0807-2025. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-0807-2025. Source: US FDA. Licensed CC0.

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