Medline LF4418CRRecalls & reported problems
Medline Industries, Inc. · LIGASURE IMPACT FT10 COMPATIBLE · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 3
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10888277680449), received between Sep 16, 2026 and Sep 30, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (3 reports).
3 FDA recall records name this device's identifier, 3 still open.
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
Recalls naming this device
- Oct 1, 2025Open, Classified
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Z-0469-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- May 7, 2024Open, Classified
Potential for an incomplete seal on the packaging tray.
Z-3094-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Aug 3, 2023Open, Classified
Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
Z-0119-2024 · Root cause: Packaging · Recall details · FDA record ↗
Most reported problems
Device problems
- Loose or Intermittent Connection3
- Communication or Transmission Problem1
- Electrical /Electronic Property Problem1
- Failure to Seal1
- Key or Button Unresponsive/not Working1
- Mechanical Jam1
- Mechanical Problem1
- Retraction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952692 ↗MalfunctionSep 29, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938321 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937901 ↗MalfunctionSep 25, 2026Loose or Intermittent Connection; Key or Button Unresponsive/not Working
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50902653 ↗MalfunctionSep 25, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50902404 ↗MalfunctionSep 24, 2026Communication or Transmission Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890028 ↗MalfunctionSep 22, 2026Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50859883 ↗MalfunctionSep 16, 2026Retraction Problem; Failure to Seal
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794883 ↗
Other Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed devices
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- Medline LF1944CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls12 reports
- MEDLINE LF1837CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls4 reports
- Medline LF1844CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls1 report
- N/A LF1837Stryker Sustainability Solutions, Inc. · ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED70 reports
- MEDLINE LF1212ACRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed1 recall8 reports
- MEDLINE LF1637CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed1 recall0 reports
- MEDLINE LF1923CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed1 recall0 reports
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 · each recall links to the FDA recall notice
- 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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