MAUDE Adverse Event Report: ETHICON INC. PDSII CLR 27IN 3-0 S/A SH; SUTURE, SURGICAL, ABSORBABLE

Catalog Number	Z416H
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).The device history records were reviewed and the manufacturing criteria was met prior to the release of this lot.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 that a patient underwent a tissue excision on an unknown date and suture was used.During the procedure, the needle tip broke off.The tip was recovered.Another like device was used to complete the procedure.There were no patient consequences reported.No additional information was available.

• Brand Name: PDSII CLR 27IN 3-0 S/A SH
• 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: 7970634
• Report Number: 2210968-2018-76578
• Device Sequence Number: 1255316
• Product Code: NEW
• UDI-Device Identifier: 10705031060852
• UDI-Public: 10705031060852
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: N18331
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 09/18/2018

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: 09/30/2022
• Device Catalogue Number: Z416H
• Device Lot Number: MGZ897
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 09/18/2018
• Initial Report FDA Received Date: 10/16/2018
• Patient Sequence Number: 1