Class II
Medical Device Recall: Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069W
MICROspecialties, Inc. · June 5, 2024
Reason for Recall
Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
Distribution
MO
States Affected
MO
Quantity Affected
804 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2336-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.