United States Surgical Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3 (2.5mm) DST Series Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3 (2.5mm) DST Series
Brand
United States Surgical
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
LOT# P2J507 P2J972 P2K1034 P2K616 P2L334 P2L335 P2L607 P2M694 P2M695 P3A83 P3B307 P3D245 P3D564 P3E236 P3E309 P3F683 P3G300 P3G855 P3H21 P3J263 P3J408 P3J42 P3K13 P3L1011 P3L1012 P3L1133 P3L1134 P3L13 P3L237 P3L447 P3L628 P3L728 P3M558 P3M668 P4A636 P4B176 U2H11 U2H17 U2J01 U2J02
United States Surgical is recalling Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3 (2.5mm) DST Series 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