MAUDE Adverse Event Report: ETHICON INC. VCL+ UD 8X18IN 2-0 S/A CP-2 CR; SUTURE, ABSORBABLE, SYNTHETIC

Catalog Number	VCP762D
Medical Device Problem Code	Device Markings/Labelling Problem (2911)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/01/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Product complaint # = > (b)(4).H6 component code: g07002 - device not returned this report is being submitted pursuant to the provisions of 21 cfr, part 803, part 4 subpart b.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by ethicon, or its employees that the report constitutes an admission that the product, ethicon, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.A manufacturing record evaluation was performed for the finished device lot, and no non-conformances were identified.Attempts have been made to retrieve the device.To date the device has not been returned.If the device or further details are received at a later date a supplemental medwatch will be sent.Additional information was requested, and the following was obtained via: - please confirm the number of patients affected by this alleged deficiency.0 - have any of these events been previously reported to ethicon? if so, provide the respective reference number(s).No * if not, please create a new pc file for each patient/event.- how many devices demonstrated the alleged deficiency? 12 boxes - are there any photos available of the product label for visual analysis? yes, see attached - please confirm if the devices are available for product analysis.If yes, please provide the status of the devices as they have not been received for analysis.If the devices have been shipped, please provide the shipment tracking details.Pictures only.- provide the source or name and title of external person providing answers to follow-up (external person submitting answers to sales rep).(please refer to the attached mail).
Event or Problem Description
It was reported that a patient underwent an unknown procedure in 2025 and suture was used.Before use on the patient, it was reported by account contact that multiple sutures of the same lot with issues on the qr code.½ have been able to scan and ½ have not been able to due to blur on edges.There was no patient consequence reported.Unknown if the device was available for return.No adverse patient consequences were reported.Additional information was requested.

• Brand Name: VCL+ UD 8X18IN 2-0 S/A CP-2 CR
• Common Device Name: SUTURE, ABSORBABLE, SYNTHETIC
• Manufacturer (Section D): ETHICON INC.; 1000 route 202; raritan NJ 08869
• Manufacturer (Section G): ETHICON INC.-JUAREZ; calle durango #2751; ciudad juarez 32575 ; MX 32575
• Manufacturer Contact: orla o'mahony ; 1000 route 202; raritan, NJ 08869 ; 3035526892
• MDR Report Key: 22396734
• Report Number: 2210968-2025-07865
• Device Sequence Number: 4799691
• Product Code: GAM
• UDI-Device Identifier: 10705031055391
• UDI-Public: (01)10705031055391(17)300131(10)106L8R
• Combination Product (Y/N): Y
• Initial Reporter Country: US
• PMA/510(K) Number: K032420
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/03/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: VCP762D
• Device Lot Number: 106L8R
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/09/2025
• Initial Report FDA Received Date: 07/03/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/21/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown