FDAJune 5, 2024device
Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
What to do
FDA enforcement status: Ongoing
Brands named
microspecialties
UPCs
10841305101064
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDASynergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 180612024-06-05
- FDASynergetics I Pack Injection Kit Custom-Tray for use with Ophthalmic injections Model/Catalog Number: 18069 Product Description:2024-06-05
- FDASynergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069W2024-06-05
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