Smith & Nephew Grasper, Cupped 3.4mm REF: 011014
FDA device recall Z-0973-05 · posted 2005-07-07 · Terminated
Recall details
- Recalling firm
- Smith & Nephew, Inc., Endoscopy Div.
- Reason for recall
- Cupped Grasper Handle marked incorrectly as Duckbill Upbiter
- Action taken
- Smith & Nephew Endoscopy notified users by letter dated 4/6/05. Accounts are requested to return product.
- Root cause
- Other
- Status
- Terminated
- Product code
- GDJ
- Quantity affected
- 12
- Distribution
- CA, OH, MA, TX
- Date initiated
- 2005-04-06
- Date posted
- 2005-07-07
- Date terminated
- 2006-06-07
- Location
- Mansfield, MA
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