Tuohy 1150-6M091Recalls & reported problems
Pajunk GmbH Medizintechnologie · Tuohy with spec.Point,1cm grad. 17G x 3 1/2" (90mm), plastic stylet · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048223130421), received between Jul 15, 2026 and Jul 15, 2026 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2026Break
(B)(4). THIS INCIDENT TOOK PLACE IN USA. REACHING OUT TO SHARE THAT WE HAD AN ISSUE WITH AN EPIDURAL NEEDLE TODAY. DURING AN INSERT THE STYLET SNAPPED OFF AT THE HUB, AND THE STYLET WAS LODGED WITHIN THE NEEDLE. FORTUNATELY, THE NEEDLE WAS REMOVED FROM THE PATIENT'S BACK AND THE STYLET REMAINED WITHIN THE NEEDLE. I HAVE THE NEEDLE AND LOT # ON HAND. ASIDE FROM REQUIRING A SECOND INSERTION ATTEMPT, THERE WERE NO FURTHER COMPLICATIONS FOR THIS PATIENT. SECOND ATTEMPT TO REINSERT A NEW NEEDLE WITH STYLET SUCCESSFUL. THE PATIENT IS DOING WELL; THE COMPLETE NEEDLE WITH STYLET WAS SUCCESSFULLY REMOVED IN ITS ENTIRETY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25826486 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.