It was determined that the deflection length indicated on the Guide catheter handle does not match the label on the box and sterile packaging for two lots.
It was determined that the deflection length indicated on the Guide catheter handle does not match the label on the box and sterile packaging for two lots.
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 Medtronic Vascular, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-3227-2017 — Medtronic Vascular, Inc. Medtronic Vascular, Inc. recalls Medtronic Aptus Heli-FX Thoracic EndoAnch Hello, I own a Medtronic Vascular, Inc. recalls Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm, REF HG-18-90-42, STERILE EO, Rx Only The that is covered by recall Z-3227-2017 from Medtronic Vascular, 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.
