Fresh Recalls

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

⚠ Recalls found. Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR is named in 7 official recalls in our current data:

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR

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.

Company / brand: Medtronic Perfusion Systems

Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR

Official ID Z-2222-2026 · Official record ↗

See all Medtronic Perfusion Systems recalls →

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.