RecallRadar

FDA Device recall Z-1458-2024

Covidien Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT

On 2024-04-10 the FDA classified a Class II recall of Covidien Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT by Covidien, citing under certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The issue is related to components i….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1458-2024
ClassificationClass II
Statusongoing
Initiated2024-02-14
Published2024-04-10
Last updated2026-09-13 11:57 UTC
CompanyCovidien
DistributionUS

Product

Covidien Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT

Reason

Under certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The issue is related to components in impacted reloads that are not fully secure, which leads to uncontrolled articulation. The issue can occur using either the Endo GIA" Ultra Universal Stapler or Signia" Stapling System.

Identifiers

code_infoModel Number: SIGSDS30CTVT; UDI/DI: 10884521741888; Lot numbers: N3L1909UY, N3L1868UY, N3L2008UY, N3L2221UY, N3M1541UY, N3M1603UY, N3M1639UY;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1458-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.