# FDA device recall: Medtronic DLP Retrograde Cannula   Manual-Inflate   Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular cat

> recall · VERIFIED · 2026-04-21

Firm: Medtronic Perfusion Systems · Class II · Certain lots of product have the potential for a sterile barrier breach.

- Company: Medtronic Perfusion Systems
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED.