MAUDE Adverse Event Report: COVIDIEN LP LLC NORTH HAVEN V-LOC 180; SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID

Model Number	VLOCL0123
Medical Device Problem Code	Unraveled Material (1664)
Health Effect - Clinical Codes	Wound Dehiscence (1154); Injury (2348); No Code Available (3191)
Date of Event	07/17/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
According to the reporter, during an abdominoplasty procedure, the two products were used on the skin when an opening occurred in the lip of the patient in the healing process.There was rupture/ break off during usage of the devices.This resulted in extended surgical time of more than 30 minutes and extended incision to more than 1 inch.The device replaced with a new one to complete the case.
Additional Manufacturer Narrative
(b)(4).Evaluation summary: post market vigilance (pmv) led an evaluation of one device.The visual inspection and functional testing confirmed there were no abnormalities that would have caused or contributed to the reported condition.A review of the device history record indicates this product was released meeting all quality release specifications at the time of manufacture.The investigation concluded there were no abnormalities that would have caused or contributed to the reported condition.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
According to the reporter, during abdominoplasty procedure, the two products were used on the skin when an opening occurred in the lip of the patient in the healing process.There was rupture/ break off during usage of the devices.This resulted to extended surgical time of more than 30 mins and extended incision to more than 1 inch.The device was replaced with a new one to complete the case.An additional operation will be done to correct the issue.
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
According to the reporter, during abdominoplasty procedure, the two products were used on the skin when an opening occurred in the lip of the patient in the healing process.There was rupture/ break off during usage of the devices.This resulted to extended surgical time of more than 30 mins and extended incision to more than 1 inch.The device was replaced with a new one to complete the case.Re-suture was done to correct the issue.
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.

• Brand Name: V-LOC 180
• Common Device Name: SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
• Manufacturer (Section D): COVIDIEN LP LLC NORTH HAVEN; 195 mcdermott rd; north haven CT 06473
• MDR Report Key: 7756515
• Report Number: 1219930-2018-04292
• Device Sequence Number: 11214862
• Product Code: GAM
• UDI-Device Identifier: 20884521130538
• UDI-Public: 20884521130538
• Combination Product (Y/N): N
• Initial Reporter Country: TU
• PMA/510(K) Number: K091087
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 10/18/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 10/31/2019
• Device Model Number: VLOCL0123
• Device Catalogue Number: VLOCL0123
• Device Lot Number: A6K0512VFX
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/10/2018
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/17/2018
• Supplement Date Received by Manufacturer: 08/08/2018; 09/12/2018; 09/25/2018
• Initial Report FDA Received Date: 08/07/2018
• Supplement Report FDA Received Date: 10/02/2018; 10/11/2018; 10/18/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention