NAMIC 90701722Recalls & reported problems
Medline Industries, Inc. · PML 72 ADULT FLL-MLL PG · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489068351), received between Jul 28, 2026 and Jul 28, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Crack” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Crack1
- Leak/Splash1
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.
MalfunctionJul 28, 2026Crack; Leak/Splash
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50060109 ↗
Other MONITOR, LINE ISOLATION devices
- NAMIC 80641962Medline Industries, Inc. · MONITOR, LINE ISOLATION1 recall1 report
- NAMIC 80641722Medline Industries, Inc. · MONITOR, LINE ISOLATION1 recall0 reports
- NAMIC 90701482Medline Industries, Inc. · MONITOR, LINE ISOLATION2 reports
- NAMIC 90701122Medline Industries, Inc. · MONITOR, LINE ISOLATION2 reports
- NAMIC 80641482Medline Industries, Inc. · MONITOR, LINE ISOLATION2 reports
- NAMIC 90701362Medline Industries, Inc. · MONITOR, LINE ISOLATION2 reports
- NAMIC 90701482Navilyst Medical, Inc. · MONITOR, LINE ISOLATION1 report
- NAMIC 80641242Navilyst Medical, Inc. · MONITOR, LINE ISOLATION1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.