SonoBlock 001180-77Recalls & reported problems
Pajunk GmbH Medizintechnologie · SonoBlock 21G (0,80) x 100mm with injection tube · 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 14048223018733), received between Aug 23, 2018 and Aug 23, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
- Improper or Incorrect Procedure or Method1
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.
MalfunctionAug 23, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
(B)(4). OBESE FEMALE PATIENT. FEMORAL BLOCK. UNDER ULTRASOUND. RESIDENT. THE NEEDLE HAS A SLIGHT BEND NEXT TO THE HUB. THE RESIDENT PUSHED DOWN VERY HARD WITH THE PROBE TO BE ABLE TO SEE THE IMAGE. IMAGE WAS OCCLUDED DUE TO FAT. THE NEEDLE CURVED AROUND THE PROBE AND CAUSED A BEND IN THE NEEDLE. WHEN THE DOCTOR WENT TO RETRIEVE THE NEEDLE, THE NEEDLE WAS DISLODGED FROM THE HUB AND STAYED INSIDE THE PATIENT. THERE WAS ANOTHER PROCEDURE TO REMOVE THE BENT NEEDLE. THE NEEDLE BENT AND BROKE OFF FROM THE HUB DUE TO EXTREME ULTRASOUND PRESSURE.
Patient problems: Device Embedded In Tissue or Plaque; Foreign Body In Patient
MAUDE report 7808032 ↗
Other NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) devices
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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.