MAUDE Adverse Event Report: ETHICON INC. PRLNE BLU 30IN 5-0 S/A RB-1; SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE

Catalog Number	8870H
Medical Device Problem Code	Material Separation (1562)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	01/01/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).Additional information was requested and the following was obtained: all the devices where used on the same procedure and had the same issue.Note: events reported via mw #2210968-2019-88804, 2210968-2019-88805, 2210968-2019-90896, 2210968-2019-90897, 2210968-2019-90898, 2210968-2019-90899, 2210968-2019-90900.
Additional Manufacturer Narrative
(b)(4).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.Attempts are being made to obtain the following information.To date no response has not been provided.If further details are received at a later date a supplemental medwatch will be sent.Sample return status ? lot #? what do you mean by "the suture brakes from the needle on this lot" ? please provide specific quality issue noticed with the suture-needle device? did the suture break into 2 pieces very close to the swage location? or did the whole suture thread pull off /separate/detach from the whole needle ? when was the reported issue noticed ? pre-op-before use on patient? or intra-op-during use on patient while suturing? confirm the total qty of devices actually involved and noticed with reported issue ?.
Event or Problem Description
It was reported that the patient underwent an unknown surgery on an unknown date and suture was used.The suture breaks from the needle on this lot.There were no adverse consequences to the patient.
Additional Manufacturer Narrative
(b)(4).A manufacturing record evaluation was performed for the finished device mhh809 batch number, and no non-conformances were identified.Additional investigation summary: it was received for analysis an opened box with unopened samples of product code 8870, lot mhh809.The complaint sample was not returned for evaluation.During the visual inspection of samples, no defects were found on the packages.The samples were opened, and the swage and attachment area were noted to be as expected.The sutures were dispensed without problems and examined along of the strands and no defects were observed.A functional test was performed and the pull force were above the minimum requirements.The manufacturing records were reviewed, and the manufacturing/packaging criteria were met prior to the release of this batch.Per the condition of the samples, no pull off suture needle was found, and the tested samples met the finished goods requirements.Additional information was requested and the following was obtained: lot # mhh809.Please provide specific quality issue noticed with the suture-needle device? the sutures separates from the needle any time the surgeons tried to pull the needle out of the skin.Did the suture break into 2 pieces very close to the swage location? or ----did the whole suture thread pull off /separate/detach from the whole needle ? second option.When was the reported issue noticed ? pre-op-before use on patient? or intra-op-during use on patient while suturing? second option.Confirm the total qty of devices actually involved and noticed with reported issue ? 7 sutures were used, 29 are remaining in the box.Attempts are being made to obtain the following information.To date no response has been provided.If further details are received at a later date a supplemental medwatch will be sent.Did all 7 devices used in the procedure experience the reported issue of suture pulling off the needle? or were 7 devices used in the procedure and 2 of the 7 experienced the reported issue of suture pulling off the needle? note: events reported via mw #2210968-2019-88805.

• Brand Name: PRLNE BLU 30IN 5-0 S/A RB-1
• Common Device Name: SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
• Manufacturer (Section D): ETHICON INC.; p.o. box 151, route 22 west; somerville NJ 08876
• MDR Report Key: 9207286
• Report Number: 2210968-2019-88804
• Device Sequence Number: 19609860
• Product Code: GAW
• UDI-Device Identifier: 10705031021525
• UDI-Public: 10705031021525
• Combination Product (Y/N): N
• Initial Reporter Country: SZ
• PMA/510(K) Number: K133356
• 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,Followup,Followup
• Report Date (Section B): 09/24/2019

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: 06/30/2023
• Device Catalogue Number: 8870H
• Device Lot Number: MHH809
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/13/2019
• Initial Date Received by Manufacturer: 09/24/2019
• Supplement Date Received by Manufacturer: 11/05/2019; 12/02/2019
• Initial Report FDA Received Date: 10/18/2019
• Supplement Report FDA Received Date: 11/22/2019; 12/13/2019
• Patient Sequence Number: 1