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Medtronic Perfusion Systems
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Type Company Card addedAugust 10 Threat lists flagged Reviews1
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Threat lists · flagged Product safety recall
Official safety regulators published alerts about a product of this kind.
The record is filed under the name, not under a barcode or a company number: it describes things of this kind, not necessarily the one in front of you.
Alerts on record48 HazardMedtronic received reports of pinhole leaks in the wire-wound body of 22 Fr EOPA 3D Arterial Cannulae and EOPA Elongated One-Piece Arterial Cannulae used during cardiopulmonary bypass proced First alertFebruary 7, 2024 Latest alertJune 24, 2026 On our lists sinceAugust 10, 2026
What to do: Check the maker, the batch and the date of the exact item you have — the alert is about this kind of product.
Where this came from: openFDA device recalls — An official government safety register — product recalls and safety alerts.
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Reviews · 1
Medtronic Perfusion Systems matters to operating rooms, where heart-lung bypass and related perfusion equipment have to work cleanly and reliably under pressure. By our assessment, its value is in highly specialized hardware and support for procedures that cannot be casual about timing or control. That makes it a serious industrial medical name rather than a consumer one, and the products are judged by precision, compatibility, and the demands of surgical workflow. The trade-off is simple: this is not broad, friendly equipment for everyone, and it only makes sense in a narrow clinical setting with trained staff. In practice, companies in this space are about machine stability, disposables, and the unglamorous discipline of not failing when the room is already busy. Compared with general medical-device brands, Medtronic Perfusion Systems sits in a narrower and more technical corner, and that narrowness is exactly what gives it weight.
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