MONOMAX VIOLET 2/0 (3) 150CM HR26 B0041444

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-18 for MONOMAX VIOLET 2/0 (3) 150CM HR26 B0041444 manufactured by B. Braun Surgical, S.a..

Event Text Entries

[183921818] Analysis and results: there are no previous complaints of this code-batch. We have received two cases regarding the same issue from the same customer (this report is for the second case). We manufactured and distributed in the market 1,992 units of this code-batch. There are no units in our stock. We have received 5 closed samples for analysis to analyze both cases. Tightness test to the samples received has been performed and the units are tight. We have tested the knot pull tensile strength of the samples received and the results fulfil the requirements of the european pharmacopoeia (ep): 3. 81 kgf in average and 3. 46 kgf in minimum (ep requirements: 2. 73 kgf in average and 1. 37 kgf in minimum). Reviewed the batch manufacturing record of this product, there are no incidences related to this issue and the results during the process fulfil usp/ep and b. Braun surgical requirements. Remarks: when working with monomax suture materials great care should be taken to ensure that the use of surgical instruments, such as tweezers and needle holders do not damage the material by being pinched or kinked. Final conclusion: although the results of the samples received fulfil the specifications of european pharmacopoeia/ b. Braun surgical specifications, we take note of this incidence in order to assess if new or additional actions are needed. 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. Corrective/preventive actions: according to our internal procedures, there is no need to establish corrective or preventive actions. Nevertheless, this complaint is recorded for trending analysis to assess if actions are needed in the future.
Patient Sequence No: 1, Text Type: N, H10


[183921819] It was reported that there was an issue with monomax suture. The client reported that the thread breaks very easily when knotting. It occurred during abdominal closure in two different surgeries and two different surgeons. No delay in surgery and patient outcome as good (this report is for the second patient). Additional information has not been provided
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003639970-2020-00169
MDR Report Key9848048
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-18
Date of Report2020-03-18
Date Mfgr Received2020-03-02
Device Manufacturer Date2018-10-29
Date Added to Maude2020-03-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS S OR
Manufacturer StreetCARRETERA DE TERRASSA, 121
Manufacturer CityRUB 08191
Manufacturer CountrySP
Manufacturer Postal08191
Manufacturer G1B. BRAUN SURGICAL, S.A.
Manufacturer StreetCARRETERA DE TERRASSA, 121
Manufacturer CityRUB 08191
Manufacturer CountrySP
Manufacturer Postal Code08191
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMONOMAX VIOLET 2/0 (3) 150CM HR26
Generic NameSYNTHETIC ABSORBABLE MONOFILAR SUTURE
Product CodeNWJ
Date Received2020-03-18
Returned To Mfg2020-03-10
Model NumberB0041444
Catalog NumberB0041444
Lot Number118441
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerB. BRAUN SURGICAL, S.A.
Manufacturer AddressCARRETERA DE TERRASSA, 121 RUB?, 08191 SP 08191


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-18

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