# FDA recall Z-1805-2024

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

## Product

Medtronic Venous Cannulae:    a)	DLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,   b)	DLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,   c)	DLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128,   d)	DLP¿ 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130,   e)	DLP¿ 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134,   f)	DLP¿ 12 Fr. Single Stage Venous Cannula, Model Number 67312,   g)	DLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67316,   h)	DLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67516,   i)	DLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 66118,   j)	DLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 67318,   k)	DLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67320,   l)	DLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 69320,   m)	DLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67520,   n)	DLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 66122

## Reason for recall

Potential for unsealed sterile packing.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1805-2024
- **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-1805-2024

## Citation

> AI Analytics. FDA recall Z-1805-2024. Retrieved 2026-07-07 from https://api.ai-analytics.org/recall/Z-1805-2024. Source: US FDA. Licensed CC0.

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