Medline LF1844CRRecalls & reported problems
Medline Industries, Inc. · LIGASURE BLUNT TIP 44CM FT10 COMPATIBLE · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888277680418), received between Sep 25, 2026 and Sep 25, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
2 FDA recall records name this device's identifier, 2 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. How this data works · Data updated Oct 13, 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-0474-2026 · Root cause: Under Investigation by firm · FDA record ↗
- Aug 3, 2023Open, Classified
Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
Z-0117-2024 · Root cause: Packaging · FDA record ↗
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50902607 ↗
Other Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed devices
- Medline LF4418CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed3 recalls8 reports
- Medline LF1937CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls13 reports
- 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
- 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 LF4318CRMedline 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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