FDA Adverse Event Injury Summary report: N

CANGAROO ENVELOPE

MDR report key: 10436005 · Received August 21, 2020

Report

Report Number
3005619880-2020-00041
Event Type
Injury
Date Received
August 21, 2020
Date of Event
July 23, 2020
Report Date
August 21, 2020
Manufacturer
AZIYO BIOLOGICS INC.
Product Code
FTM
UDI-DI
00859389005034
PMA / PMN Number
K192616
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

MANUFACTURING REVIEW OF THE CANGAROO ENVELOPE DEVICE HISTORY RECORD FOR THE REPORTED LOT SHOWS THAT ALL PACKAGED AND LABELED UNITS WERE QUALITY RELEASED TO DISTRIBUTION ON 03/03/2020 HAVING MET ALL INTERNAL QC ACCEPTANCE REQUIREMENTS. ALL STERILIZATION PROCESSING RECORDS AND BIOBURDEN TESTING INDICATE A SUCCESSFUL STERILIZATION CYCLE AND PASSING RESULTS OF PRODUCT LAL AND STERILITY SAMPLES ALLOWING THE SUBASSEMBLY LOT TO BE RELEASED FOR FURTHER PACKAGING AND LABELING HAVING MET ALL CRITERIA FOR RELEASE. THERE WERE NO NON-CONFORMANCES DURING MANUFACTURING OR STERILIZATION POTENTIALLY IMPACTING THE FINAL ACCEPTANCE OF THIS MANUFACTURING LOT. IN LIEU OF A REQUEST FOR THE OEM SUPPLIER DHR REVIEW, IT IS NOTED THAT AZIYO PROCESSES THE NON-STERILE ENVELOPE MATERIALS INCLUDING CUTTING, SUTURING, PACKAGING AND STERILIZING THE PRODUCT. IT IS ALSO NOTED THAT PER THE INSTRUCTIONS FOR USE (IFU - ART-20662) PROVIDED WITH THE FINISHED CANGAROO ENVELOPE DEVICE, INFECTION IS LISTED AS A POTENTIAL COMPLICATION ASSOCIATED WITH THE PROCEDURE AND DEVICE. ALTHOUGH THE EXACT CAUSE OF THE REPORTED INFECTION CANNOT BE CONCLUSIVELY DETERMINED, INFECTION IS A KNOWN COMPLICATION ASSOCIATED WITH THE USE OF A CANGAROO ENVELOPE AND A SURGICAL IMPLANT PROCEDURE. SHOULD AZIYO RECEIVE ANY ADDITIONAL DETAILS RELATED TO THIS EVENT, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED BY AZIYO BIOLOGICS' BUSINESS PARTNER BOSTON SCIENTIFIC, THAT A CANGAROO ENVELOPE (MODEL CMCV-009-MED LOT# M20C1091) WAS USED WITH A BOSTON SCIENTIFIC DEVICE (MODEL #/SERIAL # UNKNOWN) AND IMPLANTED ON (B)(6) 2020. PATIENT DEVELOPED AN INFECTION AND ON (B)(6) 2020 THE ENTIRE SYSTEM WAS EXPLANTED. A NEW SYSTEM WAS IMPLANTED AT THE SAME TIME ON THE OPPOSITE SIDE OF PATIENT'S CHEST. THE PATIENT WAS TREATED WITH INTRAVENOUS ANTIBIOTICS AND HAS SINCE RECOVERED. THE ISSUE WAS REPORTED TO AZIYO BIOLOGICS ON 7/24/2020 WITH ADDITIONAL DETAIL PROVIDED ON 8/05/2020.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
902678 CANGAROO ENVELOPE MESH, SURGICAL - FTM FTM AZIYO BIOLOGICS INC. CMCV-009-MED M20C1091 00859389005034

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention BSC CIED (MODEL# / SERIAL# - UNKNOWN)