Veritas Advanced Fluidics and Infusion Pack
Last updated
Summary
Product
Veritas Advanced Fluidics and Infusion Pack
Issue
Medical devices - Performance issue
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Veritas Advanced Fluidics Pack |
All lots. |
VRT-AF |
Veritas Advanced Infusion Pack |
All lots. |
VRT-AI |
Issue
Johnson & Johnson Surgical Vision, Inc. is initiating this new recall due to a manufacturing issue with Veritas packs which could result in a weld protrusion, which is the physical gap between the housing and cover of the Veritas packs, that exceeds the design specification.
Recall start date: June 2, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ophthalmology
Companies
Johnson & Johnson Surgical Vision, Inc.
31 Technology Drive, Irvine, California, United States, 92618
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73826
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