# FDA recall Z-2619-2023

> **R A Medical Services** · Class II · device recall initiated 2023-08-23.

## Product

MINISCAV (tm) Vacuum Pump

## Reason for recall

Inadequate documentation of acceptance activity

## Distribution

Distribution to Ohio

## Key facts

- **Recall number:** Z-2619-2023
- **Recalling firm:** R A Medical Services
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-23
- **Report date:** 2023-09-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Keighley, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2619-2023

## Citation

> AI Analytics. FDA recall Z-2619-2023. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2619-2023. Source: US FDA. Licensed CC0.

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