MAUDE Adverse Event Report: ETHICON INC. VCL CT BRD UD 8X18IN 0 S/A CT-1 CR; SUTURE, ABSORBABLE, SYNTHETIC

Catalog Number	J840D
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	08/01/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).A manufacturing record evaluation was performed for the finished device pcm943 batch number, and no non-conformances were identified.Attempts are being 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: did the needle pull off the suture thread and the same needle broke off the swaged portion, during final stitch? it was noted as missing the swaged portion but i believe the suture pulled off the swaged end as well.Please explain ' it was noticed one of the other needles had a needle tip missing.' was the device with the broken tip a second device used on the patient in the same procedure? yes it was a 2nd needle for the same procedure.Please explain- 'searching the floor both pieces were found.' were the two needle pieces found on the floor, one that had the broken swage part and the other broken needle tip? yes.This report is in response to (b)(4).Note: events reported via (b)(4).
Event or Problem Description
It was reported via user facility medwatch form (b)(4) that the patient underwent laparoscopic total hysterectomy and bilateral laparoscopic salpingectomy on an unknown date and suture was used.It was noticed the needle had a needle tip missing.Upon searching the floor, the needle piece was found.There were no adverse patient consequences reported.
Additional Manufacturer Narrative
(b)(4).A failed suture needle was submitted for fractographic evaluation.A fracture was observed in the body.The needle was received in two pieces, only one of the mating fracture surface was examined for this evaluation.A microscope was used to examine the fracture surface and surrounding area of the needle.The fracture surface was examined in multiple locations in order to determine the fracture mode.The evaluation revealed the fracture was composed of microvoid coalescence, which is evidence of a ductile overload failure.Mechanical damage, a cup-and-cone shaped fractures and macroscopic plastic deformation observed coincidental to the fracture provide additional evidence that the failure was induced by mechanical deformation leading to ductile overload.This was a ductile fracture.The manufacturing records were reviewed, and the manufacturing/packaging criteria were met prior to the release of this batch.The evidence of this examination indicates that the breakage occurred from mechanical deformation, indents and scratches, due to gripping, bending and overstressing of the needle.There is no evidence of any material flaw that would cause premature failure.

• Brand Name: VCL CT BRD UD 8X18IN 0 S/A CT-1 CR
• Common Device Name: SUTURE, ABSORBABLE, SYNTHETIC
• Manufacturer (Section D): ETHICON INC.; p.o. box 151, route 22 west; somerville NJ 08876 0151
• MDR Report Key: 9131483
• Report Number: 2210968-2019-88204
• Device Sequence Number: 16722571
• Product Code: GAM
• UDI-Device Identifier: 10705031043237
• UDI-Public: 10705031043237
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• PMA/510(K) Number: K022269
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: User Facility
• Report Source: health professional,other,use
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 09/03/2019

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: 02/29/2024
• Device Catalogue Number: J840D
• Device Lot Number: PCM943
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/24/2019
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: 10/24/2019
• Initial Report FDA Received Date: 09/27/2019
• Supplement Report FDA Received Date: 11/13/2019
• Patient Sequence Number: 1
• Patient Age: 48 YR
• Patient Weight: 81