TELEFLEX IPN929096Recalls & reported problems
Teleflex Incorporated · Titan SGS Stapler With Titan SGS Standard Staple-Line Reinforcement · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14026704923523), received between May 13, 2025 and Aug 4, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Firing Problem” (1 report).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Firing Problem1
- Lack of Effect1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 4, 2026Lack of Effect
Patient problems: Insufficient Information
MAUDE report 50134574 ↗MalfunctionMay 13, 2025Firing Problem; Firing Problem
IT WAS REPORTED "PUSHER BARS DID NOT PUSH UP STAPLES. NO STAPLES FIRED ON SPECIMEN SIDE". ADDITIONAL INFORMATION STATES THAT THE PROCEDURE WAS COMPLETED WITH ANOTHER STAPLER. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22012607 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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