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Mul-T-Blanket 8001-061-701Recalls & reported problems

Stryker Corporation · Class 2

All models of Mul-T-Blanket (4)

Data updated Oct 18, 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 07613327175097), received between May 9, 2018 and Jul 17, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (2 reports).

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.

Most reported problems

Device problems

  • Fluid/Blood Leak2

Patient problems

  • No Known Impact Or Consequence To Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 17, 2018Fluid/Blood Leak

    IT WAS REPORTED THAT THE BLANKET LEAKED WATER DURING USE WITH A PATIENT. NO ADVERSE CONSEQUENCES OR CLINICALLY SIGNIFICANT DELAYS IN TREATMENT WERE REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7695804 ↗
  • MalfunctionMay 9, 2018Fluid/Blood Leak

    IT WAS REPORTED THERE WAS A LEAK AT THE EDGE OF THE BLANKET WHERE THE HOSE IS LOCATED, WHICH COULD RESULT IN LIQUID LEAKING ONTO THE PATIENT SUPPORT SURFACE AREA. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7498828 ↗

Other System, thermal regulating devices

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Sources and updates

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