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Recall Observatory FDA recall evidence

Device product

Veritas Advanced Infusion Packs, REF: VRT-AI

Z-1005-2023

December 07, 2022

Class II

Product summary

Firm
Johnson & Johnson Surgical Vision, Inc.
Event
Event 91290
Status
Ongoing
Classification
Class II
Quantity
3133
Official record key
device-enforcement:Z-1005-2023

Official wording

Reason: Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.

Code information: UDI-DI/Lots: 05050474700901/60400378, 60401981, 60401982

Distribution pattern: US: FL, MS, NY, TN, TX, IL, MN, OH. OUS: Belgium, China, Estonia, France, Germany, Indonesia, Italy, Japan, Malaysia, Netherlands, Portugal, Sri Lanka, Switzerland, Thailand, United Kingdom

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.