GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for Circular Staplers, 25mm; Catalog number: 1BSGC25;
FDA Recall Z-2513-2024 · Posted 2024-08-06
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Recalling FirmW.L. Gore & Associates, Inc.
Recall StatusOpen, Classified
Product CodeFTL
Date Initiated2024-07-03
Product Quantity51 units
Reason for Recall
Devices were labeled with an expiration date of four years and ten days rather than the validated two years.
Firm Action
On July 1, 2024 URGENT MEDICAL DEVICE RECALL letters were sent to customers. Actions to be taken by the customer/user: 1. Identify and return any unused devices within the scope of this recall for replacement. 2. Please complete and sign the enclosed CUSTOMER RESPONSE FORM and return to [email protected] within 2 weeks of receipt of this notification. 3. This notice needs to be shared with those who should be aware within your institution or to any organization where potentially affected devices have been transferred (as appropriate). 4. If a listed device has been used, there is no patient follow-up needed and no further actions required other than informing Gore the device was used. Please indicate the used device(s) on the CUSTOMER RESPONSE FORM and return to [email protected]. In the event that an adverse event occurs:
Any adverse event involving the GORE SEAMGUARD Bioabsorbable Staple Line
Reinforcement Configured for Circular Staplers should be reported to W. L. Gore &
Associates and the country specific regulatory authorities immediately. To report an
event to W. L. Gore & Associates, email: [email protected] or contact:
USA: 800 528 1866 Ext. 44922 / 928 864 4922, Fax 928 864 4364
Healthcare professionals and consumers may report adverse events or quality
problems directly to FDA using the FDA MedWatch Website:
https://www.accessdata.fda.gov/scripts/medwatch/index.cfm
As a reminder, there is no known additional risk to patients who have been treated with a GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for Circular
Staplers that is subject to this voluntary recall. We regret any confusion or inconvenience
this matter may cause. Please be assured that Gore is committed to ensuring top product
quality and customer satisfaction and will be implementing actions as appropriate.
Please contact your local Gore Field Sales Associate with any questions regarding this
notice, and to coordinate the return and replacement
Root Cause
Process control
Distribution Pattern
US Nationwide distribution in the states of CA, GA, IL, NC, OH, OK, WA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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