Atlas FDA

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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