Mul-T-Pad 8002-062-026 (UDI 07613327261318)Recalls & reported problems
Stryker Corporation · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613327261318), received between Mar 23, 2018 and Apr 26, 2019 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (6 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
- Leak/Splash6
- Fluid/Blood Leak1
Patient problems
- No Consequences Or Impact To Patient4
- No Known Impact Or Consequence To Patient3
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 26, 2019Fluid/Blood Leak; Fluid/Blood Leak
THIS REPORT SUMMARIZES 3 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE BLANKET WAS LEAKING AT THE PATIENT SITE. THERE WAS PATIENT INVOLVEMENT, HOWEVER THERE WERE NO CONSEQUENCES OR IMPACTS TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8554971 ↗MalfunctionMar 23, 2018Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE TEMPERATURE THERAPY PAD IS LEAKING. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7365087 ↗MalfunctionMar 23, 2018Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE TEMPERATURE THERAPY PAD IS LEAKING. 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 7365085 ↗MalfunctionMar 23, 2018Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE TEMPERATURE THERAPY PAD IS LEAKING. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7365082 ↗MalfunctionMar 23, 2018Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE TEMPERATURE THERAPY PAD IS LEAKING. 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 7365081 ↗MalfunctionMar 23, 2018Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE TEMPERATURE THERAPY PAD IS LEAKING. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7365080 ↗MalfunctionMar 23, 2018Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE TEMPERATURE THERAPY PAD IS LEAKING. 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 7365079 ↗
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- DONJOY 11-1424Djo, LLC · Pack, hot or cold, water circulating1 recall0 reports
- T/Pump TP700Stryker Corporation · Pack, hot or cold, water circulating15 reports
- MEDLINE MDSCC20Medline Industries, Inc. · Pack, hot or cold, water circulating5 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
- 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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