Covidien LP LigaSure Atlas 20 cm Open Procedure Vessel Sealer/Divider Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LigaSure Atlas 20 cm Open Procedure Vessel Sealer/Divider
Brand
Covidien LP
Lot Codes / Batch Numbers
Catalog Number LS1120. Lot numbers: Any lot number beginning with N2, N3, N4, or N5A through N5L235K.
Products Sold
Catalog Number LS1120. Lot numbers: Any lot number beginning with N2, N3, N4, or N5A through N5L235K.
Covidien LP is recalling LigaSure Atlas 20 cm Open Procedure Vessel Sealer/Divider due to Sealing cycle may be interrupted during vessel ligation procedure, resulting in an incomplete seal.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sealing cycle may be interrupted during vessel ligation procedure, resulting in an incomplete seal.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 01/27/2006.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026