FDA Adverse Event Injury Summary report: N

PATTERSON

MDR report key: 54922 · Received December 12, 1996

Report

Report Number
1412902-1996-00004
Event Type
Injury
Date Received
December 12, 1996
Date of Event
November 18, 1996
Report Date
December 11, 1996
Manufacturer
MPL TECHNOLOGIES, INC.
Product Code
DZM
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

DURING A LOWER MANDIBULAR BLOCK ANESTHETIC INJECTION, DR. WITHDREW NEEDLE AND REALIZED IT WAS BROKEN OFF AT THE HUB. THE NEEDLE WAS EMBEDDED IN THE PT'S GUM TISSUE. DR WAS UNABLE TO REMOVE THE NEEDLE AND CONSULTED A SURGEON TO REMOVE IT. THERE WERE NO REPORTED COMPLICATIONS AND THE PT HAS FULLY RECOVERED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PATTERSON DENTAL NEEDLE DZM MPL TECHNOLOGIES, INC. PP57830 12527

Patients

Seq Age Sex Outcome Treatment
1 4 YR Required Intervention