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