SPROTTE® 071151-30ARecalls & reported problems
Pajunk GmbH Medizintechnologie · SPROTTE® 24G x 123mm, sterile, · 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 14048223000615), received between Mar 20, 2018 and Mar 20, 2018 — 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.
Most reported problems
Device problems
- Break1
- Entrapment of Device1
- Fracture1
Patient problems
- Device Embedded In Tissue or Plaque1
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 20, 2018Fracture; Break; Entrapment of Device; Fracture
(B)(4). MALE PATIENT (B)(6). DR (B)(6) TRIED TO PERFORM A SPINAL BUT STRUGGLED TO GET CSF AND CORRECT PLACEMENT OF THE NEEDLE. DR (B)(6) THEN HELPED AND TRIED WITH ANOTHER NEEDLE (ITS NOT SURE IF THE NEEDLE THAT SNAPPED WAS (B)(4)) ON PERFORMING THE SPINAL THE STYLET WAS REMOVED SUCCESSFULLY BUT NO CSF WAS FOUND. SPINAL NEEDLE WAS REMOVED, ON REMOVING IT WAS NOTICED THE END OF THE NEEDLE WAS MISSING. X RAY WAS CARRIED OUT ON THE PATIENT BUT COULD NOT BE FOUND. CT SCAN WAS CARRIED OUT AND THE POSITION OF THE TIP IDENTIFIED. MR (B)(6) VASCULAR SURGEON SUCCESSFULLY REMOVED THE BROKEN NEEDLE.
Patient problems: Device Embedded In Tissue or Plaque; Foreign Body In Patient
MAUDE report 7352292 ↗
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- ARROW IPN922605Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- 22G 1 1/2IN Regional Block Needle 408348Becton, Dickinson And Company · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN923597Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922631Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922604Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- BD QUINCKE Spinal Needles 405180Becton, Dickinson And Company · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)23 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.