FDA Adverse Event Malfunction Summary report: N

GLEN RESURFACING REAMER D27 MM

MDR report key: 4944846 · Received July 28, 2015

Report

Report Number
1818910-2015-26633
Event Type
Malfunction
Date Received
July 28, 2015
Date of Event
July 14, 2015
Report Date
July 14, 2015
Manufacturer
DEPUY FRANCE SAS 3003895575
Product Code
LXH
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED. (B)(4).

Additional Manufacturer Narrative · 1

THE DEVICES ASSOCIATED TO THE COMPLAINT WERE RETURNED FOR ANALYSIS. THE DHR ANALYSIS OF THE CONCERNED BATCHES SHOWS THAT THE LABELS WERE PRINTED ON THE SAME DAY, DECEMBER 8TH, 2011 FOR BOTH BATCHES. 2 SUPPLEMENTARY LABELS WERE REPRINTED FOR BATCH 5111794 DUE TO A PRINTING ISSUE. BASED ON THE INFORMATION RECEIVED AND THE INVESTIGATIONS PERFORMED, THE ROOT CAUSE OF THE INCIDENT IS RELATED TO A SUPPLIER LABELING ERROR. A PREVIOUS COMPLAINT WAS REPORTED FOR THIS ISSUE (B)(4). SUPPLIER CORRECTIVE ACTIONS WERE IMPLEMENTED IN 2012 THROUGH THE CAPA (B)(4). DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Description of Event or Problem · 1

I HAVE JUST BEEN PASSED THIS PRODUCTS FROM KIT BUILD AS IT LOOKS TO BE THE WRONG ITEM IN THE PACKET.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
489247 GLEN RESURFACING REAMER D27 MM SHOULDER INSTRUMENT/TRIAL LXH DEPUY FRANCE SAS 3003895575 5112868

Patients

Seq Age Sex Outcome Treatment
1