Dieckmann G05312Recalls & reported problems
Cook Incorporated · Dieckmann Intraosseous Infusion Needle 45 Degree Trocar - Pediatric Use (Less than 24 months) · Class 2
Data updated Oct 13, 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 00827002053120), received between Dec 17, 2018 and Dec 17, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Break1
- Fluid/Blood Leak1
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.
MalfunctionDec 17, 2018Fluid/Blood Leak
IT WAS REPORTED THAT THE DIECKMANN INTRAOSSEOUS INFUSION NEEDLE LUERLOCK CONNECTION WAS LEAKING. THERE WERE NO ADVERSE EFFECTS REPORTED DUE TO THE EVENT AND NO REPORT OF AN ADDITIONAL PROCEDURE. THIS COMPLAINT IS RELATED TO MFR# 1820334-2018-03778.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8170789 ↗MalfunctionDec 17, 2018Break
IT WAS REPORTED THAT DURING THE PUNCTURE OF THE TIBIA WITH THE INTRAOSSEOUS NEEDLE, THE TIP WAS BREAKING OFF. THERE WERE NO ADVERSE EFFECTS REPORTED DUE TO THE EVENT AND NO REPORT OF AN ADDITIONAL PROCEDURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8170639 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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