LIQUIFIX PRECISION
Received Jun 11, 2026 · Event occurred May 12, 2026
Report 9617175-2026-00061 · MDR key 25471362
Device
Generic name
Tissue Adhesive For Internal Use
Manufacturer
Advanced Medical Solutions LtdModel number
72014033Lot number
UNK
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Skin Infection
Narrative
Additional Manufacturer Narrative
THE ADVERSE EVENT WAS RECEIVED AS PART OF THE US POST APPROVAL STUDY (PAS).= FROM THE AACHQC REGISTRY. AS SUCH NO FURTHER DETAILS CAN BE ACQUIRED INCLUDING TO A LOT NUMBER TO ENABLED A DETAILED INVESTIGATION. DETAILS RECEIVED FROM THE ACHQC WERE: 1 X SURGICAL SITE INFECTION. A. TIME: 1 YEAR FOLLOW UP B. DEVICE: LIQUIFIX PRECISION 72014033 C. LOCATION: USA. AS PER FDA 21 CFR 803.3, A 'SERIOUS INJURY' IS DEFINED AS: 'AN INJURY OR ILLNESS THAT: · IS LIFE THREATENING; · RESULTS IN PERMANENT IMPAIRMENT OF A BODY FUNCTION OR PERMANENT DAMAGE TO A BODY STRUCTURE; OR · NECESSITATES MEDICAL OR SURGICAL INTERVENTION TO PRECLUDE PERMANENT IMPAIRMENT OF A BODY FUNCTION OR PERMANENT DAMAGE TO A BODY STRUCTURE. AS AN SSI IS AN INFECTION THAT USUALLY REQUIRES MEDICAL INTERVENTION TO PRECLUDE PERMANENT IMPAIRMENT OF A BODY FUNCTION OR PERMANENT DAMAGE TO A BODY STRUCTURE, THIS EVENT IS BEING REPORTED.
Description of Event or Problem
1 X SURGICAL SITE INFECTION. A. TIME: 1 YEAR FOLLOW UP B. DEVICE: LIQUIFIX PRECISION 72014033 C. LOCATION: USA.