Endo GIA 030459Recalls & reported problems

Summary

The FDA's MAUDE database contains 651 adverse event reports that list this exact device (DI 10884523002904), received between May 15, 2017 and Apr 28, 2026 — classified as 1 death, 165 injuries, 485 malfunctions.

The most frequently reported specific device problem is “Failure to Form Staple” (339 reports).

73 other recalls cover devices cleared under the same FDA submission (K111825); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 651 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 28, 2026Misfire

  ACCORDING TO THE REPORTER DURING A PARTIAL LOBECTOMY, THERE WERE FIRING ISSUES. A NEW RELOAD WAS USED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25011769 ↗
• MalfunctionMar 23, 2026Failure to Fire

  IT WAS REPORTED THAT DURING A THORACOSCOPIC RIGHT LOWER LOBECTOMY, WHEN DETACHING THE PULMONARY HILUM AND PULMONARY VEIN, THE TWO RELOADS FIRING WERE OBSTRUCTED. THE ISSUE WAS RESOLVED BY REPLACING THE RELOADS. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660724 ↗
• MalfunctionNov 20, 2025Difficult to Open or Close; Difficult to Open or Close

  ACCORDING TO THE REPORTER, DURING A THORACOSCOPIC PARTIAL RESECTION OF THE APICOPOSTERIOR SEGMENT AND MEDIAL SEGMENT OF THE RIGHT UPPER LOBE AND THE ANTERIOR BASAL SEGMENT OF THE LOWER LOBE, THE RELOAD WAS USED WITH THE STAPLER, BUT THE RELOAD COULD NOT BE CLOSED AND COULD NOT BE USED PROPERLY. A NEW RELOAD OF THE SAME SPECIFICATION AND MODEL WAS REPLACED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23604720 ↗
• MalfunctionSep 19, 2025Misfire; Firing Problem; Misfire; Firing Problem

  IT WAS REPORTED THAT DURING A LOW ANTERIOR RESECTION (LAR) PROCEDURE, THERE WAS DIFFICULTY FIRING THE TWO RELOADS WHEN USED WITH A MANUAL HANDLE. THE PROCEDURE WAS EXTENDED BY 30 MINUTES AS A RESULT. THE DEVICE WAS REPLACED WITH ANOTHER COMPANY'S PRODUCT. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT. MEDTRONIC'S INITIAL EVALUATION OF THE INCIDENT DEVICE FOUND THE LOADING UNIT WAS PARTIALLY FIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23096708 ↗
• MalfunctionJul 22, 2025Failure to Form Staple; Failure to Form Staple

  ACCORDING TO THE REPORTER, DURING A THORACOSCOPIC WEDGE RESECTION OF THE LUNG, AT THE BEGINNING, WHILE USING THE FIRST HANDLE AND RELOAD, THE STAPLES WERE POORLY FORMED AND IT BURST OUT. A SECOND RELOAD WAS USED WITH THE FIRST HANDLE, AND DURING FIRING, THE STAPLER PUSHED HALFWAY AND COULD NOT CONTINUE TO PUSH. THE SURGEON CONTINUED TO PUSH, AND A LOUD, ABNORMAL SOUND WAS HEARD. A SECOND HANDLE AND THIRD RELOAD WERE USED; THE STAPLER PUSHED HALFWAY AND COULD NOT CONTINUE TO PUSH; THE RESISTANCE WAS VERY LARGE; AND AN ABNORMAL SOUND WAS HEARD, BUT THE SURGEON WAS NOT SURE IF IT WAS DAMAGED. A FOURTH RELOAD WAS USED WITH THE SECOND HANDLE, AND DURING FIRING, IT COULD NOT BE PUSHED, AND THE HANDLE WAS DAMAGED. A PURPLE RELOAD WAS USED WITH THE SECOND HANDLE, AND DURING FIRING, IT COULD NOT BE PUSHED, AND THE HANDLE WAS DAMAGED. THE SURGEON REPLACED THE HANDLE AND USED THE SAME PURPLE RELOAD, BUT DURING FIRING, IT PUSHED HALFWAY, AND IT COULD NOT CONTINUE TO PUSH. SURGICAL TIME WAS EXTENDED BY ABOUT 30 MINUTES. THE SURGEON MANUALLY SUTURED THE TISSUE TO RESOLVE THE ISSUE. THE SURGEON USED ANOTHER BRAND OF STAPLER TO COMPLETE THE CASE.

  Patient problems: Tissue Breakdown

  MAUDE report 22566468 ↗
• MalfunctionJul 22, 2025Misfire; Misfire

  ACCORDING TO THE REPORTER, DURING A THORACOSCOPIC WEDGE RESECTION OF THE LUNG, AT THE BEGINNING, WHILE USING THE FIRST HANDLE AND RELOAD, THE STAPLES WERE POORLY FORMED AND IT BURST OUT. A SECOND RELOAD WAS USED WITH THE FIRST HANDLE, AND DURING FIRING, THE STAPLER PUSHED HALFWAY AND COULD NOT CONTINUE TO PUSH. THE SURGEON CONTINUED TO PUSH, AND A LOUD, ABNORMAL SOUND WAS HEARD. A SECOND HANDLE AND THIRD RELOAD WERE USED; THE STAPLER PUSHED HALFWAY AND COULD NOT CONTINUE TO PUSH; THE RESISTANCE WAS VERY LARGE; AND AN ABNORMAL SOUND WAS HEARD, BUT THE SURGEON WAS NOT SURE IF IT WAS DAMAGED. A FOURTH RELOAD WAS USED WITH THE SECOND HANDLE, AND DURING FIRING, IT COULD NOT BE PUSHED, AND THE HANDLE WAS DAMAGED. A PURPLE RELOAD WAS USED WITH THE SECOND HANDLE, AND DURING FIRING, IT COULD NOT BE PUSHED, AND THE HANDLE WAS DAMAGED. THE SURGEON REPLACED THE HANDLE AND USED THE SAME PURPLE RELOAD, BUT DURING FIRING, IT PUSHED HALFWAY, AND IT COULD NOT CONTINUE TO PUSH. SURGICAL TIME WAS EXTENDED BY ABOUT 30 MINUTES. THE SURGEON MANUALLY SUTURED THE TISSUE TO RESOLVE THE ISSUE. THE SURGEON USED ANOTHER BRAND OF STAPLER TO COMPLETE THE CASE.

  Patient problems: Tissue Breakdown

  MAUDE report 22566380 ↗
• MalfunctionJul 22, 2025Misfire; Misfire

  ACCORDING TO THE REPORTER, DURING A THORACOSCOPIC WEDGE RESECTION OF THE LUNG, AT THE BEGINNING, WHILE USING THE FIRST HANDLE AND RELOAD, THE STAPLES WERE POORLY FORMED AND IT BURST OUT. A SECOND RELOAD WAS USED WITH THE FIRST HANDLE, AND DURING FIRING, THE STAPLER PUSHED HALFWAY AND COULD NOT CONTINUE TO PUSH. THE SURGEON CONTINUED TO PUSH, AND A LOUD, ABNORMAL SOUND WAS HEARD. A SECOND HANDLE AND THIRD RELOAD WERE USED; THE STAPLER PUSHED HALFWAY AND COULD NOT CONTINUE TO PUSH; THE RESISTANCE WAS VERY LARGE; AND AN ABNORMAL SOUND WAS HEARD, BUT THE SURGEON WAS NOT SURE IF IT WAS DAMAGED. A FOURTH RELOAD WAS USED WITH THE SECOND HANDLE, AND DURING FIRING, IT COULD NOT BE PUSHED, AND THE HANDLE WAS DAMAGED. A PURPLE RELOAD WAS USED WITH THE SECOND HANDLE, AND DURING FIRING, IT COULD NOT BE PUSHED, AND THE HANDLE WAS DAMAGED. THE SURGEON REPLACED THE HANDLE AND USED THE SAME PURPLE RELOAD, BUT DURING FIRING, IT PUSHED HALFWAY, AND IT COULD NOT CONTINUE TO PUSH. SURGICAL TIME WAS EXTENDED BY ABOUT 30 MINUTES. THE SURGEON MANUALLY SUTURED THE TISSUE TO RESOLVE THE ISSUE. THE SURGEON USED ANOTHER BRAND OF STAPLER TO COMPLETE THE CASE.

  Patient problems: Tissue Breakdown

  MAUDE report 22566337 ↗
• InjuryJul 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE LITERATURE, A RETROSPECTIVE STUDY ASSESSED ONE ANASTOMOSIS GASTRIC BYPASS (OAGB) AS A REVISIONAL SURGERY AFTER FAILED VERTICAL BANDED GASTROPLASTY (VBG). IN ALL 71 PROCEDURES PERFORMED BETWEEN FEBRUARY 2014 AND FEBRUARY 2020, A GREEN STAPLER WAS USED TO CREATE THE GASTRIC POUCH. ONE PATIENT (1.4%) DEVELOPED AN ANASTOMOTIC STRICTURE FOLLOWING SURGERY, WHICH WAS TREATED WITH UPPER GI ENDOSCOPY AND BALLOON DILATATION. THIS COMPLICATION WAS CLASSIFIED AS A SERIOUS INJURY. OTHER POSTOPERATIVE EVENTS INCLUDED BLEEDING, LEAKAGE, ABSCESS, WOUND INFECTION, BILE REFLUX, GASTRIC ULCER, AND HERNIA.

  Patient problems: Abscess; Failure to Anastomose; Hemorrhage/Blood Loss/Bleeding; Stenosis; Unintended Radiation Exposure

  MAUDE report 22475569 ↗
• MalfunctionMay 16, 2025Failure to Form Staple; Failure to Form Staple

  ACCORDING TO THE REPORTER, DURING A SINGLE-PORT THORACOSCOPIC LOBECTOMY (RIGHT UPPER LOBE) PLUS REGIONAL LYMPH NODE RESECTION, AFTER CUTTING THE LUNG TISSUE, THE STAPLE BURST OUT AND BLEED. A DIFFERENT TYPE OF RELOAD WAS THEN USED, BUT THE STAPLE BURST OUT AGAIN. THIS ISSUE CAUSED TISSUE DAMAGE. TO RESOLVE THE ISSUE, ANOTHER STAPLER WAS USED. HEMOSTASIS AT THE BLEEDING SITE AND MONITORING OF THE PATIENT'S VITAL SIGNS DURING THE SURGERY WERE STRENGTHENED. IT WAS NOTED THAT THE PROCEDURE TIME WAS EXTENDED.

  Patient problems: Hemorrhage/Blood Loss/Bleeding; Tissue Breakdown

  MAUDE report 22040682 ↗
• MalfunctionMay 5, 2025Failure to Form Staple; Failure to Form Staple

  IT WAS REPORTED THAT DURING A SURGICAL PROCEDURE, THERE WERE ISSUES WITH INCOMPLETE STAPLE LINES AFTER FIRING. THE DEVICES WERE REPLACED TO RESOLVE THE ISSUE.

  Patient problems: Tissue Breakdown

  MAUDE report 21961322 ↗
• InjuryMay 5, 2025Break; Entrapment of Device; Human-Device Interface Problem; Break; Entrapment of Device; Human-Device Interface Problem

  IT WAS REPORTED THAT DURING A TOTAL GASTRECTOMY PROCEDURE, THE RELOAD BECAME STUCK WITH THE ADAPTER, NECESSITATING A CONVERSION TO AN OPEN PROCEDURE. IT WAS ALSO NOTED THAT THE RELOAD COULD BE REMOVED FROM THE ADAPTER, BUT THE TIP WAS BROKEN.

  Patient problems: Laceration(s)

  MAUDE report 21958635 ↗
• MalfunctionApr 22, 2025Failure to Form Staple; Failure to Fire; Failure to Form Staple; Failure to Fire

  IT WAS REPORTED THAT DURING A SURGICAL PROCEDURE, INVOLVING GREEN AND BLACK RELOAD, THERE WERE ISSUES WITH INCOMPLETE STAPLE LINES AFTER FIRING. THIS RESULTED IN AN EXTENDED SURGICAL TIME. THE DEVICES WERE REPLACED TO RESOLVE THE ISSUE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; Tissue Breakdown

  MAUDE report 21885520 ↗
• MalfunctionMar 27, 2025Misfire; Misfire

  IT WAS REPORTED THAT DURING A COLECTOMY, THERE WERE FIRING ISSUES WITH THE RELOAD COMPONENT OF THE STAPLER. THE MANUAL HANDLE WAS SQUEEZED PARTIALLY AND STOPPED WORKING EVEN THOUGH THE TISSUE WASN'T TOO THICK. A NEW RELOAD WAS USED ON THE SAME STAPLER, AND IT FIRED NORMALLY. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21708720 ↗
• MalfunctionMar 13, 2025Failure to Form Staple; Failure to Form Staple

  IT WAS REPORTED THAT DURING A LAPAROSCOPIC RADICAL GASTRIC CANCER SURGERY, THERE WERE PROCEDURAL ISSUES INVOLVING THE MANUAL STAPLER. THERE WAS POOR STAPLE FORMATION WITH THE INABILITY TO FORM A PERFECT B SHAPE. THE DEVICE WAS BEING APPLIED TO THE STOMACH AT THE TIME OF THE ISSUE. TWO RELOADS WERE USED WITH THE SAME ISSUE. THE PROBLEM WAS RESOLVED BY REPLACING THE PRODUCT WITH A NEW ONE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; Tissue Breakdown

  MAUDE report 21595279 ↗
• MalfunctionJan 20, 2025Failure to Form Staple; Failure to Form Staple

  ACCORDING TO THE REPORTER, DURING A RADICAL LUNG CANCER SURGERY, THE FIRST RELOAD HAD POOR STAPLE FORMATION AND STAPLE LINE INCOMPLETE ISSUE. THE SECOND RELOAD HAD AN UNKNOWN ISSUE. THE DEVICE WAS REPLACED TO COMPLETE THE PROCEDURE.

  Patient problems: Tissue Breakdown

  MAUDE report 21191768 ↗
• MalfunctionJan 16, 2025Failure to Form Staple; Failure to Form Staple

  ACCORDING TO THE REPORTER DURING A LAPAROSCOPIC GASTRIC SURGERY, THE STAPLES BURST OUT CAUSING THE CUTTING TO FAIL AND THE RUPTURE OF THE PATIENT'S GASTRIC WALL IN THE SURGICAL AREA. IT OCCURRED ON TWO RELOADS. TO RESOLVE THE ISSUE, MANUAL SUTURING AND SEROMUSCULAR LAYER EMBEDDING REINFORCEMENT WERE DONE.

  Patient problems: Tissue Breakdown

  MAUDE report 21170527 ↗
• MalfunctionJan 16, 2025Failure to Form Staple; Failure to Form Staple

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC GASTRIC SURGERY, THE STAPLES BURST OUT, CAUSING THE CUTTING TO FAIL AND THE RUPTURE OF THE PATIENT'S GASTRIC WALL IN THE SURGICAL AREA. IT OCCURRED ON TWO RELOADS. TO RESOLVE THE ISSUE, MANUAL SUTURING AND SEROMUSCULAR LAYER EMBEDDING REINFORCEMENT WERE DONE.

  Patient problems: Tissue Breakdown

  MAUDE report 21169189 ↗
• MalfunctionJan 10, 2025Failure to Fire; Failure to Fire

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC SLEEVE GASTRECTOMY, ON THE FIRST FIRING AT THE PYLORUS, THE TWO RELOADS COULD NOT BE FIRED WHEN IT WAS FIRED TO THE MIDDLE POSITION. TO RESOLVE THE ISSUE, A NEW STAPLER WAS USED, AND A MANUAL SUTURING WAS DONE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21130157 ↗
• MalfunctionJan 2, 2025Failure to Form Staple; Failure to Form Staple

  ACCORDING TO THE REPORTER DURING A PROCEDURE, THE RELOAD BURST WHEN THE LAPAROSCOPIC LINEAR CUTTING STAPLER WAS USED TO CUT THE LUNG TISSUE.

  Patient problems: Tissue Breakdown

  MAUDE report 21053881 ↗
• MalfunctionNov 27, 2024Failure to Form Staple; Detachment of Device or Device Component; Failure to Form Staple; Detachment of Device or Device Component

  ACCORDING TO THE REPORTER, DURING A THORACOSCOPIC SEGMENTECTOMY, WHEN REMOVAL OF LUNG TISSUE, THE STAPLER WAS ABLE TO FIRE, THE STAPLES WERE NOT COMPLETELY STAPLED ON THE LUNG, AND ALL OF THEM FELL OFF, AND THE STAPLE LINE WAS INCOMPLETE CENTRALLY. ANOTHER RELOAD WAS USED, BUT SAME ISSUE OCCURRED. A REPLACEMENT DEVICE FROM ANOTHER MANUFACTURER WAS DONE TO RESOLVE THE ISSUE.

  Patient problems: Tissue Breakdown

  MAUDE report 20803007 ↗
• MalfunctionNov 27, 2024Failure to Form Staple; Detachment of Device or Device Component; Failure to Form Staple; Detachment of Device or Device Component

  ACCORDING TO THE REPORTER, DURING A THORACOSCOPIC SEGMENTECTOMY, WHEN REMOVAL OF LUNG TISSUE, THE STAPLER WAS ABLE TO FIRE, THE STAPLES WERE NOT COMPLETELY STAPLED ON THE LUNG, AND ALL OF THEM FELL OFF, AND THE STAPLE LINE WAS INCOMPLETE CENTRALLY. ANOTHER RELOAD WAS USED, BUT SAME ISSUE OCCURRED. A REPLACEMENT DEVICE FROM ANOTHER MANUFACTURER WAS DONE TO RESOLVE THE ISSUE.

  Patient problems: Tissue Breakdown

  MAUDE report 20801221 ↗
• MalfunctionNov 27, 2024Failure to Form Staple; Adverse Event Without Identified Device or Use Problem; Failure to Form Staple; Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, DURING AN ESOPHAGEAL CANCER PROCEDURE, THREE RELOADS HAD STAPLE LINE INCOMPLETE, AND TWO OF THE RELOADS HAD STAPLE LINE DID NOT HOLD OR OPENED UP. THE SURGICAL TIME WAS EXTENDED. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20800691 ↗
• MalfunctionNov 27, 2024Failure to Form Staple; Adverse Event Without Identified Device or Use Problem; Failure to Form Staple; Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, DURING A PROCEDURE, THREE RELOAD HAD STAPLE LINE INCOMPLETE, AND TWO OF THE RELOAD HAD STAPLE LINE DID NOT HOLD OR OPENED UP, THE SURGICAL TIME WAS EXTENDED. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20800662 ↗
• MalfunctionNov 18, 2024Misfire; Failure to Form Staple; Failure to Fire; Misfire; Failure to Form Staple; Failure to Fire

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC LOBECTOMY PROCEDURE, WHEN DETACHING THE LUNG LOBE, THE STAPLE STUCK, THE STAPLE LINE INCOMPLETE PROXIMALLY. A NEW HANDLE AND RELOAD WAS USED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20708055 ↗
• MalfunctionNov 13, 2024Break; Break

  ACCORDING TO THE REPORTER, DURING A ROBOTIC LOWER ANTERIOR RESECTION, THE LOADING POINT OF THE RELOAD AND HANDLE BROKE. A NEW HANDLE AND RELOAD WAS USED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20674151 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K111825. One submission often covers many models, so check the product and lot details in each record.

• Z-0747-2021 · Nov 23, 2020 · Completed
  Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or tra
• Z-0748-2021 · Nov 23, 2020 · Completed
  Covidien TA Auto Suture Vascular Loading Unit with DST Series Technology 30 mm- V3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection
• Z-0007-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Loading Unit, Item Code 030457 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic
• Z-0003-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm, Item Code 030452 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecolo
• Z-0005-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm, Item Code 030454 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric
• Z-0004-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm, Item Code 030453 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecolo
• Z-0002-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm, Item Code 030451 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecolo
• Z-0009-2021 · Aug 12, 2020 · Open, Classified
  Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA Universal Loading Units, Parent Codes 00Z2760 - Product Usage: The Endo GIA universal staplers have applicat
• Z-0008-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm, Item Code 030458 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecolo
• Z-0006-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm, Item Code 030455 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecolo
• Z-0001-2021 · Aug 12, 2020 · Open, Classified
  Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code 030450 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gyn
• Z-1264-2020 · Jan 17, 2020 · Terminated
  Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection, transection in general surgery Item Code: EGIAUSTND
• Z-1836-2019 · May 17, 2019 · Open, Classified
  SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC , SIG60CTAMT
• Z-1825-2019 · May 17, 2019 · Open, Classified
  EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT
• Z-1834-2019 · May 17, 2019 · Open, Classified
  SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA, SIG60AXT

…and 58 more.