FDA Adverse Event Injury Summary report: N

SECHRIST INDUSTRIES, INC

MDR report key: 10828594 · Received November 12, 2020

Report

Report Number
10828594
Event Type
Injury
Date Received
November 12, 2020
Date of Event
October 21, 2020
Report Date
November 3, 2020
Manufacturer
SECHRIST INDUSTRIES, INC.
Product Code
BZR
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

WHEN THE SWEEP GAS WAS ASSESSED, THE KNOB ON LITER SIDE OF SWEEP GAS APPEARED TO BE OFF AS THE BALL USED TO GAUGE THE LEVEL OF THE SWEEP GAS WAS NOT ELEVATED. HOWEVER, THE KNOB, WHEN TURNED TO THE LEFT, WAS ABLE TO BE TIGHTENED DOWN AND TRULY TURNED OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1297053 SECHRIST INDUSTRIES, INC MIXER, BREATHING GASES, ANESTHESIA INHALATION BZR SECHRIST INDUSTRIES, INC. 3500CP-G

Patients

Seq Age Sex Outcome Treatment
1