Endo Clip IIIRecalls & reported problems across all models
Covidien LP · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2,271
- Deaths reported
- 1
- Injuries reported
- 84
- Recalls
- 0
We found 2 models of Endo Clip III by Covidien LP in the FDA's device registry (GUDID). Together they are named in 2,271 adverse event reports in the FDA's MAUDE database, received between May 10, 2016 and Sep 29, 2026 — classified as 1 death, 84 injuries, 2,186 malfunctions.
The most frequently reported specific device problem is “Mechanics Altered” (1,357 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Endo Clip III problems
Device problems
- Mechanics Altered1,357
- Mechanical Problem485
- Difficult to Open or Close267
- Detachment of Device or Device Component219
- Entrapment of Device109
- Break103
- Display or Visual Feedback Problem88
- Fail-Safe Problem79
Patient problems
- No Clinical Signs, Symptoms or Conditions1,237
- No Consequences Or Impact To Patient451
- No Known Impact Or Consequence To Patient341
- Insufficient Information170
- No Patient Involvement46
- No Information38
- Unspecified Tissue Injury32
- No Code Available30
Endo Clip III models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Endo Clip III 176630CLIP, IMPLANTABLE1 death1,959 reports
- Endo Clip III 176630BApplier, surgical, clip312 reports
Recent Endo Clip III adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Mechanics Altered; Insufficient Device Problem Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936333 ↗MalfunctionSep 29, 2026Mechanics Altered
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935770 ↗MalfunctionSep 29, 2026Difficult to Remove; Difficult to Open or Close
Patient problems: Insufficient Information
MAUDE report 50935314 ↗MalfunctionSep 29, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934957 ↗MalfunctionSep 29, 2026Mechanics Altered
It was reported that during laparoscopic gallbladder surgery, the clip applier experienced a clip loading and firing issues. A new device was used to resolve the issue. There was no patient injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934839 ↗MalfunctionSep 29, 2026Fail-Safe Problem; Mechanics Altered
It was reported that during an ear, nose, and throat (ENT) surgery, when there were seven uses remaining, the clip got stuck and the device became unusable. It was reported that the handle could not be squeezed when the issue occurred. A new device was replaced to resolve the issue. No patient complications have been reported as a result of this event. PLI 10: Medtronic's initial evaluation of the incident is that the handle was actuated and the dinks were examined and were observed to be improperly aligned.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934768 ↗MalfunctionSep 29, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933674 ↗MalfunctionSep 29, 2026Mechanics Altered; Noise, Audible
It was reported that during laparoscopic cholecystectomy and gastric bypass procedures, heard a sound during firing sequence. It seemed as if the instrument blocked itself. Customer did not want to use violence on the instrument. Another clip applier was opened to complete the procedures. There was no patient injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50927070 ↗MalfunctionSep 28, 2026Mechanics Altered
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926524 ↗MalfunctionSep 28, 2026Mechanics Altered
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926164 ↗MalfunctionSep 28, 2026Mechanics Altered; Noise, Audible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918253 ↗MalfunctionSep 24, 2026Fail-Safe Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890402 ↗MalfunctionSep 24, 2026Difficult to Open or Close
Patient problems: Insufficient Information
MAUDE report 50876581 ↗MalfunctionSep 24, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876572 ↗MalfunctionSep 22, 2026Difficult to Remove
It was reported that during a laparoscopic procedure, the surgeon was unable to remove the Endo clip without removing the port .The clip applier was fully utilized to complete the procedure . There was no patient injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50860176 ↗
Other Covidien LP products
- Endo GIA48 models · 26,277 reports · 8 recalls
- Endo GIA Ultra3 models · 15,650 reports
- Shiley387 models · 9,392 reports · 5 recalls
- Signia16 models · 8,201 reports · 6 recalls
- LigaSure32 models · 7,283 reports · 1 recall
- Tri-Staple 2.037 models · 4,892 reports · 2 recalls
- Polysorb291 models · 4,564 reports · 2 recalls
- EEA39 models · 4,432 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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