FDA Adverse Event Malfunction Summary report: N

V-LOC 90

MDR report key: 21374824 · Received February 13, 2025

Report

Report Number
1219930-2025-00739
Event Type
Malfunction
Date Received
February 13, 2025
Date of Event
January 9, 2025
Report Date
February 13, 2025
Manufacturer
COVIDIEN LP LLC NORTH HAVEN
Product Code
GAM
UDI-DI
10884521131682
PMA / PMN Number
K100257
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D10 CONCOMITANT MEDICAL PRODUCT: VLOCM0023, VLOCM0023 V-LOC* 90 4-0 CLR 45CM P12X12 (LOT#A3G1282VFY); VLOCM0023, VLOCM0023 V-LOC* 90 4-0 CLR 45CM P12X12 (LOT#A3G1282VFY); VLOCM0023, VLOCM0023 V-LOC* 90 4-0 CLR 45CM P12X12 (LOT#A3G1282VFY); MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

Description of Event or Problem · 0

ACCORDING TO THE REPORTER, DURING A RIGHT KNEE REPLACEMENT, WHEN SUTURING THE SKIN USING THE CONTINUOUS SUTURING TECHNIQUE, FOUR SUTURES BROKE. IT WAS NOTED THAT IT LASTED FIVE MINUTES. ANOTHER SUTURES WERE USED FOR RESTITCHING TO RESOLVED THE ISSUE. THERE WAS NO PATIENT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
881156 V-LOC 90 SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC AC GAM COVIDIEN LP LLC NORTH HAVEN VLOCM0023 A3G1282VFY 10884521131682

Patients

Seq Age Sex Outcome Treatment
1 62 YR Male