MAUDE Adverse Event Report: ETHICON INC. PDSII SUT 18IN(45CM) 6-0 CLR; SUTURE, SURGICAL, ABSORBABLE

Catalog Number	Z489G
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	02/06/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).A manufacturing record evaluation was performed for the finished device lot, and no non-conformances were identified.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.
Event or Problem Description
It was reported a patient underwent an unknown plastic surgery on (b)(6) 2019 a suture was used.The suture was broken at the swage part during dermostitch by continuous suturing.It was commented that no extra tensile strength was applied to the suture.Further details are not provided there were no adverse consequences to the patient.

• Brand Name: PDSII SUT 18IN(45CM) 6-0 CLR
• Common Device Name: SUTURE, SURGICAL, ABSORBABLE
• Manufacturer (Section D): ETHICON INC.; p.o. box 151, route 22 west; somerville NJ 08876 0151
• MDR Report Key: 8394366
• Report Number: 2210968-2019-79291
• Device Sequence Number: 13860179
• Product Code: NEW
• UDI-Device Identifier: 10705031061132
• UDI-Public: 10705031061132
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: N18331
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 02/07/2019

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 Expiration Date: 05/31/2023
• Device Catalogue Number: Z489G
• Device Lot Number: MGM941
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/07/2019
• Initial Report FDA Received Date: 03/06/2019
• Patient Sequence Number: 1