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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:199945

Ventralight ST w Echo PS 4.5" Circle 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: 5955450G (EU only)

Official recall number

Z-2243-2023

Evidence summary

Product code
FTL
Recall status
Open, Classified
Event initiated
April 25, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2243-2023

Field note

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