Incomplete and/or partial deployment of the CTAG Device during the endovascular procedure.
Incomplete and/or partial deployment of the CTAG Device during the endovascular procedure.
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 W L Gore & Associates, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0048-2018 — W L Gore & Associates, Inc. W L Gore & Associates, Inc. recalls GORE TAG, THORACIC ENDOPROSTHESIS, Hello, I own a W L Gore & Associates, Inc. recalls GORE TAG, THORACIC ENDOPROSTHESIS, CONFORMABLE. The GORE TAG Thoracic Endoprosthesis is intended for endovascular that is covered by recall Z-0048-2018 from W L Gore & Associates, 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.
