# FDA recall Z-1804-2024

> **Medtronic Perfusion Systems** · Class II · device recall initiated 2024-03-19.

## Product

Medtronic Suction Tubes:   a) DLP¿ Suction Tube 6-Fr. Shaft with Frazier Tip, Model Number:  10050,   b) DLP¿ Suction Tube 6-Fr. Shaft with 10-Fr. Soft Tip, Model Number:  10052,   c) DLP¿ Suction Tube 6-Fr. Shaft with 10-Fr. Soft Tip, Model Number:  10053,   d) DLP¿ Suction Tube 10 Fr. Shaft with 20 Fr. Pool Tip, Model Number:  10060,   e) DLP¿ Suction Tube 16 Fr. Shaft with 20 Fr. Fluted Tip, Model Number:  10061

## Reason for recall

Potential for unsealed sterile packing.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1804-2024
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-19
- **Report date:** 2024-05-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brooklyn Park, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1804-2024

## Citation

> AI Analytics. FDA recall Z-1804-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1804-2024. Source: US FDA. Licensed CC0.

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