FDA Medical Device Recalls (openFDA)
Covidien LP: LigaSure Atlas Laparoscopic Vessel Sealer/Divider
- Recall number
- Z-0772-06
- Recalling firm
- Covidien LP
- Product
- LigaSure Atlas Laparoscopic Vessel Sealer/Divider
- Status
- Terminated
- Initiated
- 2006-01-27
- Posted
- 2006-04-19
- Terminated
- 2008-08-15
- Reason
- Sealing cycle may be interrupted during vessel ligation procedure, resulting in an incomplete seal.
- Root cause
- Other
- Action
- Consignees were notified by letter on 01/27/2006.
- Quantity
- 124,000 units domestic, 126,000 units internationally.
- Distribution
- Nationwide, including 52 VA facilities and 12 military facilities. Foreign distribution to Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Curacao, Germany, Guatamala, Israel, Japan, Mexico, Paraguay, Peru, Singapore, South Africa, Uruguay, Venezuela.
- Lot, serial or model codes
- Catalog Number LS1100. Lot Numbers: Any lot number beginning with U, N2, N3, N4, or N5A through N5L247K.
- 510(k) numbers
- ["K010013"]
- PMA numbers
- not on file
- Product code
- GEI
- Firm FEI
- 1717344
- Firm city
- Boulder
- Firm state
- CO
- 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