Dieckmann G05986Recalls & reported problems
Cook Incorporated · Dieckmann Intraosseous Infusion Needle 45 Degree Trocar - Pediatric Use (Less than 24 months) · Class 2
- 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 00827002059863), received between Dec 17, 2018 and Dec 17, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
- Material Twisted/Bent1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 17, 2018Device Dislodged or Dislocated; Material Twisted/Bent
IT WAS REPORTED THAT WHEN THE PHYSICIAN PUNCTURED FOR THE BONE MARROW WITH INTRAOSSEOUS NEEDLE URGENTLY, IT BENT AND COULD NOT BE USED FOR TRANSFUSION. THE COMPLAINT DEVICE WAS REPLACED WITH ANOTHER DEVICE. IT WAS FURTHER NOTED THAT THE CANNULA HAD BEEN DISLODGED FROM ITS GLUE JOINT WITH THE WINGED HUB. NO OTHER INFORMATION WAS MADE AVAILABLE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8170849 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.