# FDA recall Z-0952-2026

> **Rocket Medical Plc** · Class II · device recall initiated 2025-11-07.

## Product

Brand Name: Rocket  Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray  Model/Catalog Number: R54544-18-PK  Software Version: N/A  Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices.  Component: N/A

## Reason for recall

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

## Distribution

Domestic: CO, CT, IL, MA, ME, NH, NJ, NM, OH, RI, SC, TX;  International: UAE, Austria, Australia, Canada, Germany, Denmark, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, India, Italy, Jersey, Kenya, Sri Lanka, Malta, Netherlands, Norway, New Zealand, Portugal, Saudi Arabia, Singapore, Slovenia, South Africa

## Key facts

- **Recall number:** Z-0952-2026
- **Recalling firm:** Rocket Medical Plc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-07
- **Report date:** 2025-12-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tyne & Wear, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0952-2026

## Citation

> AI Analytics. FDA recall Z-0952-2026. Retrieved 2026-07-29 from https://api.ai-analytics.org/recall/Z-0952-2026. Source: US FDA. Licensed CC0.

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