FreshRecalls

Medtronic Perfusion Systems recalls

12 recent recalls on record for Medtronic Perfusion Systems in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.

Models with recalls

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR (7)Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR (2)Octopus 4 Tissue Stabilizer (1)Octopus Evolution AS Tissue Stabilizer (1)Octopus Evolution Tissue Stabilizer (1)

All Medtronic Perfusion Systems recalls

FDA Class II · Medical device · July 1, 2026

Octopus 4 Tissue Stabilizer recall — Medtronic Perfusion Systems

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…

Official ID Z-2577-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Octopus Evolution AS Tissue Stabilizer recall — Medtronic Perfusion Systems

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…

Official ID Z-2576-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Octopus Evolution Tissue Stabilizer recall — Medtronic Perfusion Systems

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…

Official ID Z-2575-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2222-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2221-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2220-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2219-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2218-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2217-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2216-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2215-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall — Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

Official ID Z-2214-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.