Penumbra has identified an issue in these four lots involving a raw material component of the delivery wire. This issue could result in breakage of the delivery wire, which could potentially lead to serious patient injury or death.
Penumbra has identified an issue in these four lots involving a raw material component of the delivery wire. This issue could result in breakage of the delivery wire, which could potentially lead to serious patient injury or death.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Penumbra Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-2702-2017 — Penumbra Inc. Penumbra Inc. recalls Penumbra 3D Revascularization Device It is indicated for used i Hello, I own a Penumbra Inc. recalls Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic that is covered by recall Z-2702-2017 from Penumbra Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
