United States Surgical Auto SutureTA 30 Reloadable Stapler,Single Patient Use,3.5mm DST Series Ref: TA3035S Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Auto SutureTA 30 Reloadable Stapler,Single Patient Use,3.5mm DST Series Ref: TA3035S
Brand
United States Surgical
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
LOT# P2J505 P2J971 P2K1031 P2K813 P2L332 P2L603 P2L604 P2M227 P2M228 P2M235 P2M82 P3A1151 P3A323 P3A443 P3A908 P3B336 P3B607 P3C710 P3C802 P3D563 P3D944 P3E233 P3E294 P3G08 P3G09 P3G417 P3G621 P3G769 P3H288 P3H638 P3J41 P3J456 P3K05 P3K06 P3K07 P3K08 P3L1007 P3L1008 P3L11 P3L1129 P3L1130 P3L12 P3L243 P3L42 P3L425 P3L440 P3L441 P3M368 P3M369 P4A634 P4A881 U2H02 U2H08
United States Surgical is recalling Auto SutureTA 30 Reloadable Stapler,Single Patient Use,3.5mm DST Series Ref: TA3035S due to Stapler may clamp without the staples being fired into the tissue. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Stapler may clamp without the staples being fired into the tissue
Recommended Action
Per FDA guidance
United States Surgical notiied direct accounts by letter dated 5/5/04. Accounts are requested to inventory and quarantine product for return to USS.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026