Hem-o-lok Endo5 Ligation Applier
FDA device recall Z-0031-05 · posted 2004-10-22 · Terminated
Recall details
- Recalling firm
- Weck
- Reason for recall
- The jaws may break during clip loading or clip application.
- Action taken
- Consignees were notified via Federal Express (Domestic) and by email (International and Weck Sales Representatives).
- Root cause
- Other
- Status
- Terminated
- Product code
- HBT
- Quantity affected
- 119 units
- Distribution
- Nationwide; Australia, Buenos Aires, Canada, France, Korea, New Zealand, Singapore.
- Date initiated
- 2004-08-18
- Date posted
- 2004-10-22
- Date terminated
- 2005-01-31
- Location
- Research Triangle Park, NC
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