Integrated Power Supply US 15072-000-0010Recalls & reported problems
Eitan Medical Ltd · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 17290109150205), received between Jan 16, 2018 and Oct 30, 2019 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Charging Problem” (3 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
- Charging Problem3
- Power Problem1
Patient problems
- No Consequences Or Impact To Patient2
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 30, 2019Charging Problem; Charging Problem
THE EVENT WAS REPORTED BY A CUSTOMER FROM THE (B)(6): "PUMP CHARGING ISSUE DUE TO IPS PIN PROBLEM".
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9254330 ↗MalfunctionOct 30, 2019Charging Problem; Charging Problem
THE COMPLIANT WAS REPORTED BY A CUSTOMER FROM (B)(6). CHARGING ISSUE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9254256 ↗MalfunctionMar 11, 2019Charging Problem; Charging Problem
THE EVENT WAS REPORTED BY A CUSTOMER FROM USA: CHARGING ISSUE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8407628 ↗MalfunctionJan 16, 2018Power Problem; Power Problem
THE EVENT WAS REPORTED BY A CUSTOMER FROM (B)(6): POWER SUPPLY MAKES A STATIC SPARKING SOUND.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7192869 ↗
Other Accessories, Pump, Infusion devices
- Medfusion 4000-0106-01Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION2 recalls4,390 reports
- Medfusion 4000-0105-51Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION2 recalls2,882 reports
- CADD 21-2111-0401-51Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION4 recalls461 reports
- CADD 21-2112-0402-78Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION3 recalls0 reports
- MEDFUSION 4000-0106-00Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION2 recalls10 reports
- Medfusion 3500-0600-00Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION2 recalls9 reports
- Medfusion 3500-0600-51Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION2 recalls2 reports
- Medfusion 4000-0105-78Icu Medical, Inc. · ACCESSORIES, PUMP, INFUSION2 recalls0 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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