W L Gore recalls specific Heparin endoprosthesis models for packaging defects that may compromise sterility and heparin activity. Affected units include certain reference numbers and lot serial numbers.
Due to packaging defects, sterility assurance and heparin activity may be compromised.
W L Gore is recalling specific models of Heparin endoprosthesis due to packaging defects that could compromise sterility and heparin activity. This affects medical devices used in procedures like angioplasty.
Packaging defects in the endoprosthesis could lead to compromised sterility and heparin activity. This means the device might not function properly or could cause infections during medical procedures.
Patients who received the recalled endoprosthesis during procedures in the United States are affected. Medical professionals using these devices for clinical procedures are at risk if they have the specific reference numbers listed.
Check if your device has reference numbers starting with BXB055902C through BXB095902C. Look for lot serial numbers like 27342032/00733132658053 or similar combinations listed in the recall notice.
Review your device's reference number and lot serial number to confirm if it matches the recalled list.
W L Gore is recalling specific Heparin endoprosthesis models with reference numbers starting with BXB055902C through BXB095902C.
Check if your device has a reference number from the list provided (e.g., BXB055902C) and a lot serial number like 27342032/00733132658053.
The recall does not specify a remedy, so contact W L Gore directly for guidance on next steps.
We’ve drafted a message you can send W L Gore to request your refund or repair — edit it as you like.
Subject: Recall Z-2946-2024 — W L Gore W L Gore Hello, I own a W L Gore that is covered by recall Z-2946-2024 from W L Gore. 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.
