MAUDE Adverse Event Report: ETHICON INC. GUT PL UD 18IN 6-0 D/A G-1 PRM; SUTURE, ABSORBABLE, NATURAL

Model Number	770G
Medical Device Problem Code	Appropriate Device Problem Term/Code Not Available (3191)
Health Effect - Clinical Code	Cyst(s) (1800)
Date of Event	01/01/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Product complaint: (b)(4).A manufacturing record evaluation was performed for the finished device batch number, and no non-conformances were identified.Attempts are being made to clarify 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.How was the cyst in the patient #6 treated? was there any medical/surgical intervention required? additional information was requested, and the following was obtained: the patient demographic info: age, gender, weight, bmi at the time of index procedure? all children under the age of 18.Males and female.Not sure about weight.Date and name of index surgical procedure? - occurred between (b)(6) 2020 and (b)(6) 2020 on what tissue was the suture used? - conjunctiva what was the tissue condition, i.E., normal or thin, calcified, fragile, diseased? normal pediatric conjunctiva how was the suture placed (interrupted or continuous)? - interrupted how was the suture tied (square knot or multiple knots one end)? - square knot was there any precipitating stress factor for the sutures untying? - no were there any patient¿s outcome due to the post-op suture untying event? ¿ cyst did the patient require a re-suturing post-operatively? - no other relevant patient history/concomitant medications? -none what is physician¿s opinion as to the etiology of or contributing factors to this event (untying suture post-op)? not holding knot and coming untied, unclear why.How many patients had untied sutures post-op? - 5 how many patients required re-suturing post-operatively? - 0 were these post-op cases reported to ethicon before? if yes, please provide product complaint numbers.No device return status/follow up? actual defective product not available for return, only 1 package from both lot is available.Please obtain the correct product code and or lot/batch number.- lots pam087 and qamlsb the following information was requested, but unavailable: what is the patient¿s current status? post-op events for each of 5 patients were submitted via following medwatches: post-op outcome: healed okay - 2210968-2020-08057 and 2210968-2020-08058 post-op outcome: healed okay ¿ 2210968-2020-09179 and 2210968-2020-09181 post-op outcome: open conjunctival incision- 2210968-2020-09176 and 2210968-2020-09177 post-op outcome: granuloma formation- - 2210968-2020-09183 and 2210968-2020-09184 post-op outcome: cyst- 2210968-2020-09185.
Event or Problem Description
It was reported that a patient underwent an eye procedure on an unknown date between (b)(6) 2020 and (b)(6) 2020 and the suture was used interrupted and tied with square knot on normal pediatric conjunctiva tissue.The suture was not holding its knots and coming untied in the immediate post-op period.There was no precipitating stress factor for the suture untying.The patient experienced cyst and did not require re-suturing.The doctor opined that it is unclear why the suture was not holding knot and coming untied.Additional information requested.

• Brand Name: GUT PL UD 18IN 6-0 D/A G-1 PRM
• Common Device Name: SUTURE, ABSORBABLE, NATURAL
• Manufacturer (Section D): ETHICON INC.; p.o. box 151, route 22 west; somerville NJ 08876
• MDR Report Key: 10879703
• Report Number: 2210968-2020-09186
• Device Sequence Number: 19915832
• Product Code: GAL
• UDI-Device Identifier: 10705031010475
• UDI-Public: 10705031010475
• Combination Product (Y/N): N
• Initial Reporter State: CT
• Initial Reporter Country: US
• PMA/510(K) Number: K946173
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 11/09/2020

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: 12/31/2024
• Device Model Number: 770G
• Device Catalogue Number: 770G
• Device Lot Number: QAMLSB
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 11/09/2020
• Initial Report FDA Received Date: 11/20/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1