Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR: recall status

⚠ Recall found. Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR is named in 2 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 GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR

Recalls naming this model

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 ↗

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 ↗

See all Medtronic Perfusion Systems recalls →

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & egg products ↗ (not yet aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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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.