FDA Adverse Event No answer provided Summary report: N

4085 SURGICAL TABLE

MDR report key: 13839039 · Received March 21, 2022

Report

Report Number
13839039
Event Type
No answer provided
Date Received
March 21, 2022
Date of Event
March 11, 2022
Report Date
March 15, 2022
Manufacturer
STERIS CORPORATION
Product Code
FQO
Report Source
User Facility report
Reporter Location
TX
Reporter Occupation
RISK MANAGER
Health Professional
N

Narratives

Description of Event or Problem · 0

PATIENT WAS INTUBATED AND THE TEAM WAS TURNING THE BED. AN OMFS (ORAL AND MAXILLOFACIAL SURGERY) RESIDENT WAS AT THE HEAD OF THE BED WHEN THE HEADPIECE CAME OFF AND THE PATIENT'S HEAD DROPPED AND HYPEREXTENDED. ANESTHESIA GRABBED THE PATIENT'S HEAD. A C-COLLAR WAS PLACED, AND THE PATIENT WAS EXTUBATED AND TAKEN TO PACU (POST-ANESTHESIA RECOVERY UNIT) WHERE HE GOT A NEURO CONSULT AND AN MRI.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
517766 4085 SURGICAL TABLE TABLE, OPERATING-ROOM, AC-POWERED FQO STERIS CORPORATION 4085 SURGICAL TABLE

Patients

Seq Age Sex Outcome Treatment
1 7300 DA Male