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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:209372

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001658;

Official recall number

Z-2899-2024

Evidence summary

Product code
KDD
Recall status
Open, Classified
Event initiated
July 26, 2024
Root cause
No Marketing Application
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2899-2024

Field note

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