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Terminated

Auto SutureTA 30 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref: TA30348S

FDA Recall Z-0960-04 · Posted 2004-07-20

Recalling FirmUnited States Surgical
Recall StatusTerminated
Product CodeGDW
Date Initiated2004-05-05
Date Terminated2006-11-15

Reason for Recall

Stapler may clamp without the staples being fired into the tissue

Firm Action

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

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K013860AUTO SUTURE SURGICAL STAPLESUnited States Surgical, A Division of Tyco Healthc · 2001-12-19

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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