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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CELONOVA BIOSCIENCES GERMANY GMBH ONCOZENE MICROSPHERES; EMBOLIC DEVICE

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CELONOVA BIOSCIENCES GERMANY GMBH ONCOZENE MICROSPHERES; EMBOLIC DEVICE Back to Search Results
Device Problem Therapy Delivered to Incorrect Body Area (1508)
Patient Problem Not Applicable (3189)
Event Date 05/04/2016
Event Type  malfunction  
Manufacturer Narrative
Additional investigation was performed to obtain the details of the event and the potential cause(s) that resulted in the rabbit's death.Based on available information, the individual conducting the procedure injected the microsphere suspension against resistance instead of injecting the suspension in a slow-controlled manner as provided in the ifu.This resulted in embolization proximal of the treatment site or led to reflux into non-target artery.
 
Event Description
Celonova received information that on (b)(4) 2016, during a study using rabbits on the hypervascular tumor model at the (b)(6), one of five animals treated died one day post procedure.In the communication received from the study laboratory, it was noted that on (b)(6) 2016, the beads had agglomerated and plugged the catheter during treatment.A large plug of beads passed through the catheter and occluded a large portion of the liver (animal died following day).After some trouble shooting, the issue was identified - the ifu was not followed and not enough contrast was added.Therefore, the beads solution was too concentrated and the microcatheter was clogged or temporarily clogged.Embozene tandem microspheres were used in this study.Brand name is populated with oncozene microspheres, the similar product with 510(k) approval.
 
Manufacturer Narrative
This resulted in embolization proximal of the treatment site or led to reflux into non-target artery.The root cause for injecting against resistance is insufficient training of the personnel performing the animal study: no training was performed in person due to travel interruption.The training was later completed over the phone, but no follow up occurred.
 
Event Description
Celonova received information that on 04may2016, during a study using rabbits on the hypervascular tumor model at the (b)(6), one of five animals treated died one day post procedure.In the communication received from the study laboratory, it was noted that on (b)(6) 2016, the beads had agglomerated and plugged the catheter during treatment.A large plug of beads passed through the catheter and occluded a large portion of the liver (animal died following day).After some trouble shooting, the issue was identified - the ifu was not followed and not enough contrast was added.Therefore, the beads solution was too concentrated and the microcatheter was clogged or temporarily clogged.Embozene tandem microspheres were used in this study.Brand name: is populated with oncozene microspheres, the similar product with 510(k) approval.
 
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Brand Name
ONCOZENE MICROSPHERES
Type of Device
EMBOLIC DEVICE
Manufacturer (Section D)
CELONOVA BIOSCIENCES GERMANY GMBH
ernst-abbe-str. 40 d-89079
ulm,
GM 
Manufacturer (Section G)
CELONOVA BIOSCIENCES GERMANY GMBH
ernst-abbe-strausse, 40 d-8907
ulm,
GM  
Manufacturer Contact
stephanie fossat-dominguez
840 el camino real, ste.111
carlsbad, CA 92008
MDR Report Key5705546
MDR Text Key46778185
Report Number3007240980-2016-00007
Device Sequence Number1
Product Code NAJ
Combination Product (y/n)N
PMA/PMN Number
K141209
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type study
Type of Report Initial,Followup
Report Date 06/08/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/08/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Was Device Available for Evaluation? No
Date Manufacturer Received05/09/2016
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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