MEDLINE LF1212ACRRecalls & reported problems
Medline Industries, Inc. · LIGASURE SMALL JAW FT10 COMPATIBLE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names 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
- 1
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10888277680326), received between Sep 22, 2026 and Sep 30, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (3 reports).
1 FDA recall record name this device's identifier, 1 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 18, 2026.
Reports received per month
Recalls naming this device
- Oct 1, 2025Class IIOpen, 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-0470-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Electrical /Electronic Property Problem3
- Compatibility Problem1
- Component Misassembled1
- Component or Accessory Incompatibility1
- Data Problem1
- Failure to Cut1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
- Unspecified Infection1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Data Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952799 ↗MalfunctionSep 29, 2026Compatibility Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938287 ↗MalfunctionSep 28, 2026Mechanical Problem; Failure to Cut
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921585 ↗MalfunctionSep 25, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50902680 ↗MalfunctionSep 24, 2026Component or Accessory Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50889756 ↗MalfunctionSep 24, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50889610 ↗MalfunctionSep 24, 2026Electrical /Electronic Property Problem
It was reported that "It's not firing on at all."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50889592 ↗MalfunctionSep 22, 2026Component Misassembled
Patient problems: Unspecified Infection
MAUDE report 50860121 ↗
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
- 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 LF1823CRMedline 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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