FDAApril 25, 2023device

Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection

What to do

FDA enforcement status: Ongoing

Brands named

davol

UPCs

00801741031724

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450 — Recall Details · AllClear