Hem-o-lok Endo5 Ligation Applier Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hem-o-lok Endo5 Ligation Applier
Lot Codes / Batch Numbers
Catalog number 544965, Lot 943704, 943705, 954592
Products Sold
Catalog number 544965, Lot 943704, 943705, 954592
A medical device manufacturer is recalling Hem-o-lok Endo5 Ligation Applier due to The jaws may break during clip loading or clip application.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The jaws may break during clip loading or clip application.
Recommended Action
Per FDA guidance
Consignees were notified via Federal Express (Domestic) and by email (International and Weck Sales Representatives).
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