FDA Adverse Event Injury Summary report: N

HEMASORB RESORBABLE BONE PUTTY

MDR report key: 4947114 · Received July 24, 2015

Report

Report Number
3005972619-2015-00001
Event Type
Injury
Date Received
July 24, 2015
Report Date
July 23, 2015
Manufacturer
ABYRX INC,
Product Code
MTJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

A DISTRIBUTOR REPRESENTATIVE REPORTED TO ABYRX THAT A HOSPITAL HAD RECENT PROBLEMS WITH INFECTIONS. HEMASORB HAD BEEN USED BY THIS HOSPITAL DURING PROCEDURES SINCE LATE 2014 AND THEREFORE IS BEING TAKEN INTO CONSIDERATION AS PART OF THE HOSPITAL'S INVESTIGATION. THE HOSPITAL HAD PREVIOUSLY INDICATED DIFFICULTY CLEANING THEIR INSTRUMENTS FOLLOWING PROCEDURES INVOLVING HEMASORB. THE HOSPITAL BELIEVED IT HAD CORRECTED THE ISSUE BY IMPROVING THEIR CLEANING TECHNIQUE. AN ABYRX REVIEW OF THE MANUFACTURING RECORDS FOR ALL LOTS OF HEMASORB SHIPPED TO THE HOSPITAL DID NOT UNCOVER ANY IRREGULARITIES. NO INFORMATION SUPPORTS A PRODUCT MALFUNCTION OR OUT OF SPECIFICATION PRODUCT. ABYRX IMMEDIATELY REQUESTED A TELEPHONE CONVERSATION WITH THE SURGEON OR SURGICAL COORDINATOR, THROUGH THE DISTRIBUTOR REPRESENTATIVE, BUT THIS ATTEMPT AND REPEATED SUBSEQUENT ATTEMPTS (ONCE PER WEEK FROM (B)(6) 2015 TO (B)(6) 2015) WERE UNSUCCESSFUL. UNSUCCESSFUL ATTEMPTS TO REACH HOSPITAL REPRESENTATIVES VIA TELEPHONE WERE MADE ON (B)(6) 2015 ABD (B)(6) 2015 BY ABYRX. ABYRX ALSO MADE UNSUCCESSFUL EMAIL ATTEMPTS TO CONTACT THE HOSPITAL ON (B)(6) 2015 AND ON (B)(6) 2015. ADDITIONAL ATTEMPTS TO CONTACT THE USER FACILITY WILL BE MADE. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME, BUT WILL BE PROVIDED AS IT BECOMES AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
481681 HEMASORB RESORBABLE BONE PUTTY BONE WAX MTJ ABYRX INC, OS-401

Patients

Seq Age Sex Outcome Treatment
1 Other