MAUDE Adverse Event Report: B.BRAUN SURGICAL SA OPTILENE 10/0(0,2) 15CM DRM5 100MIC BLT; CARDIAC SUTURE

Model Number G3090782

Device Problems Material Integrity Problem (2978); Separation Problem (4043)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 10/25/2019

Event Type  malfunction  

Manufacturer Narrative

Pma/510k: reported device not marketed in the u.S., however, similar devices or devices that share components, raw materials, process methods or other technological characteristics are registered within the u.S.K133890.If additional information becomes available a follow up report will be submitted.

Event Description

It was reported the needle-suture has "bad fiction." the reporter indicated that the oncology surgical department is experiencing bad fiction with the needle and suture.The needle is permanently tearing from the thread.Per one surgeon, this occurred three times during a surgical procedure.It was reported that all optilene from 3/0 to 10/0, breaks at the junction of the thread with the needle; the 10/0 suture detached when removing from packaging.Per reporter, it is not possible to provide the information about every patient separately.

Manufacturer Narrative

Investigation: samples received: there are no samples available for analysis.Analysis and results: there are no previous complaints of the same code-batch.We manufactured and distributed in the market 120 units of this code-batch.There are no units in stock.We have not received any sample for analysis.Without any sample we cannot carry out an analysis in order to take a decision.Reviewed the batch manufacturing record, this product had a normal process and the results during the process fulfil usp/ep and b.Braun surgical requirements.Final conclusion: without samples we are not in position of studying if the affected product does not fulfil the specifications.In consequence, a proper analysis cannot be done and the case is not confirmed due to lack of evidence.Nevertheless, we take note of this incidence and if any sample is received in the future, we will re-open the case and analyse it.Please note that when no samples are received our analysis is very limited.Actions on product distributed of this reference/batch: based on the conclusion derived from investigation, it is not required to make actions in distributed product.No corrective/preventive actions needed.

• Brand Name: OPTILENE 10/0(0,2) 15CM DRM5 100MIC BLT
• Type of Device: CARDIAC SUTURE
• Manufacturer (Section D): B.BRAUN SURGICAL SA; 121 carretera de terrassa; rubi, 08191 ; SP 08191
• MDR Report Key: 9349634
• MDR Text Key: 172448690
• Report Number: 3003639970-2019-00799
• Device Sequence Number: 1
• Product Code: GAW
• Combination Product (y/n): N
• PMA/PMN Number: SEE H10
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup
• Report Date: 02/04/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/20/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: G3090782
• Device Catalogue Number: G3090782
• Device Lot Number: 118241
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 02/04/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1