# FDA recall Z-1813-2022

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2022-08-12.

## Product

Olympus POWERSEAL 5MM, 23CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION      Model Number: PS-0523CJDA.  An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.

## Reason for recall

An out of specification component preventing the blue retention ring from keeping the rotation knob in place. This may result in a loose rotation collar and retention ring and cause delay of treatment

## Distribution

Nationwide OUS:  AUSTRALIA,  CANADA ,  HONG KONG,  CHINA,  KOREA

## Key facts

- **Recall number:** Z-1813-2022
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-12
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1813-2022

## Citation

> AI Analytics. FDA recall Z-1813-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1813-2022. Source: US FDA. Licensed CC0.

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