IMMAGE BUFFER 3 447050 (BUFFER PART NUMBER)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2010-07-12 for IMMAGE BUFFER 3 447050 (BUFFER PART NUMBER) manufactured by Beckman Coulter Inc..

Event Text Entries

[16744391] Customer contacted beckman coulter inc. , (bci) stating that they found a loose cap on the buffer 3 image and the product leaked. No injury was reported on this issue.
Patient Sequence No: 1, Text Type: D, B5


[17124941] The customer was sent a replacement.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2050012-2010-00399
MDR Report Key1753658
Report Source05
Date Received2010-07-12
Date of Report2010-07-12
Date of Event2010-06-22
Date Mfgr Received2010-06-22
Device Manufacturer Date2010-01-29
Date Added to Maude2010-11-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMS. NORA ZEROUNIAN
Manufacturer Street250 S. KRAEMER BLVD.
Manufacturer CityBREA 92821
Manufacturer CountryUS
Manufacturer Postal92821
Manufacturer Phone7149613634
Manufacturer G1BECKMAN COULTER INC.
Manufacturer Street250 S. KRAEMER BLVD.
Manufacturer CityBREA 92821
Manufacturer CountryUS
Manufacturer Postal Code92821
Single Use0
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMMAGE BUFFER 3
Generic NameIMMAGE BUFFER 3
Product CodeCFN
Date Received2010-07-12
Model NumberNA
Catalog Number447050 (BUFFER PART NUMBER)
Lot NumberM002432
OperatorHEALTH PROFESSIONAL
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER INC.
Manufacturer Address250 S KRAEMER BLVD. BREA 92821 US 92821


Patients

Patient NumberTreatmentOutcomeDate
10 2010-07-12

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