# FDA recall Z-1793-2024

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

## Product

Medtronic Arterial Cannulae packaged as:    a)	DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020;   b)	DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220;   c)	DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020;   d)	DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120;   e)	DLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222;   f)	DLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122;   g)	DLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220;   h)	DLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222;   i)	DLP" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006;   j)	DLP" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206;   k)	DLP" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008;   l)	DLP" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010;   m)	DLP" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110;   n)	DLP" One-Piece Ped

## Reason for recall

Potential for unsealed sterile packing.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1793-2024
- **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-1793-2024

## Citation

> AI Analytics. FDA recall Z-1793-2024. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-1793-2024. Source: US FDA. Licensed CC0.

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