FDA Medical Device Recalls (openFDA)
W.L. Gore & Associates, Inc.: GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for Circular Staplers, 25mm; Catalog number: 1BSGC25;
- Recall number
- Z-2513-2024
- Recalling firm
- W.L. Gore & Associates, Inc.
- Product
- GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for Circular Staplers, 25mm; Catalog number: 1BSGC25;
- Status
- Open, Classified
- Initiated
- 2024-07-03
- Posted
- 2024-08-06
- Terminated
- not on file
- Reason
- Devices were labeled with an expiration date of four years and ten days rather than the validated two years.
- Root cause
- Process control
- 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 FieldActionTeam@wlgore.com 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 FieldActionTeam@wlgore.com. 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: medcomplaints@wlgore.com 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
- Quantity
- 51 units
- Distribution
- US Nationwide distribution in the states of CA, GA, IL, NC, OH, OK, WA.
- Lot, serial or model codes
- Catalog Number: 1BSGC25; UDI-DI: 00733132600755; Lot number: 26590654;
- 510(k) numbers
- ["K053200"]
- PMA numbers
- not on file
- Product code
- FTL
- Firm FEI
- 3003910212
- Firm city
- Elkton
- Firm state
- MD
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28