FDA Adverse Event Malfunction Summary report: N

SPHERE INFLATION DEVICE

MDR report key: 11604335 · Received April 1, 2021

Report

Report Number
1820334-2021-01050
Event Type
Malfunction
Date Received
April 1, 2021
Date of Event
March 25, 2021
Report Date
May 4, 2021
Manufacturer
COOK INC
Product Code
MAV
UDI-DI
10827002310275
PMA / PMN Number
K953522
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

THIS REPORT IS BEING SUBMITTED AS A CORRECTION. UPON FURTHER REVIEW, IT HAS BEEN DETERMINED THAT ATRION IS THE LABELED MANUFACTURER OF THE COMPLAINT DEVICE AND IS THEREFORE RESPONSIBLE FOR ALL REGULATORY REPORTING AND COMPLAINT INVESTIGATION REQUIREMENTS. THE COMPLAINT INFORMATION HAS BEEN PROVIDED TO THE MANUFACTURER (ATRION) AND ENTERED IN THE COMPLAINT FILE BY COOK INC.

Description of Event or Problem · 0

NO ADDITIONAL INFORMATION REGARDING THE PATIENT AND/OR EVENT HAS BEEN RECEIVED SINCE THE PREVIOUS MEDWATCH REPORT WAS SENT.

Additional Manufacturer Narrative · 1

COMMON DEVICE NAME: PTM ; KOE. NAME AND ADDRESS: POSTAL CODE: (B)(6). THIS REPORT INCLUDES INFORMATION KNOWN AT THIS TIME. A FOLLOW UP REPORT WILL BE SUBMITTED SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE.

Description of Event or Problem · 1

AS REPORTED, WHEN THE USER OPENED THE PACKAGE FOR A SPHERE INFLATION DEVICE, A FOREIGN WHITE SUBSTANCE WAS CONFIRMED ON THE DEVICE. THERE WAS A SMALL AMOUNT OF WHITE POWDER ON THE HANDLE AND THE GAUGE METER. THE USER WIPED IT OFF WITH GAUZE AND USED THE DEVICE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THERE WERE NO ADVERSE EFFECTS REPORTED DUE TO THIS OCCURRENCE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
501225 SPHERE INFLATION DEVICE MAV COOK INC 96271A004 10827002310275

Patients

Seq Age Sex Outcome Treatment
1