Atlas FDA

Auto SutureTA 60 Reloadable Stapler,Single Patient Use, 3.5mm DST Series Ref: TA6035S

FDA device recall Z-0963-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
United States Surgical
Reason for recall
Stapler may clamp without the staples being fired into the tissue
Action taken
United States Surgical notiied direct accounts by letter dated 5/5/04. Accounts are requested to inventory and quarantine product for return to USS.
Root cause
Other
Status
Terminated
Product code
GDW
Distribution
Nationwide
Date initiated
2004-05-05
Date posted
2004-07-20
Date terminated
2006-11-15
Location
North Haven, CT

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Related 510(k) clearances

RecordFirmDate
AUTO SUTURE SURGICAL STAPLES (K013860)United States Surgical, A Division of Tyco Healthc2001-12-19