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Recall Observatory FDA recall evidence

Device product

Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069W

Z-2336-2024

June 05, 2024

Class II

Product summary

Firm
MICROspecialties, Inc.
Event
Event 94794
Status
Ongoing
Classification
Class II
Quantity
804 units
Official record key
device-enforcement:Z-2336-2024

Official wording

Reason: Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.

Code information: UDI: 10841305101132 LOT: P62764970R

Distribution pattern: MO

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.