FDA Adverse Event Malfunction Summary report: N

CRYOMACS FREEZING BAG 750

MDR report key: 6350088 · Received February 22, 2017

Report

Report Number
3005290010-2017-00105
Event Type
Malfunction
Date Received
February 22, 2017
Date of Event
January 20, 2017
Report Date
February 22, 2017
Manufacturer
MILTENYI BIOTEC GMBH
Product Code
LPZ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT DURING THAWING OF A CRYOMACS FREEZING BAG 750 (CFB), THE CFB BROKE COMPLETELY. THE CUSTOMER STATED THAT THEY WERE ABLE TO TRANSPLANT THE PATIENT WITH SUFFICIENT CELLULAR MATERIAL. THEREFORE, ANY RISK FOR THE PATIENT COULD BE RULED OUT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
132573 CRYOMACS FREEZING BAG 750 CRYOMACS FREEZING BAG 750 LPZ MILTENYI BIOTEC GMBH N/A 6160105007

Patients

Seq Age Sex Outcome Treatment
1