FreshRecalls

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR: recall status

⚠ Recall found. Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR is named in 7 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand
Medtronic Perfusion Systems
Also listed as
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR

Recalls naming this model

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 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-2218-2026 · 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 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 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 15FR recall — Medtronic Perfusion Systems

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

Official ID Z-2222-2026 · Official record ↗

See all Medtronic Perfusion Systems recalls →

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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 3:00 AM UTC.