FDAFDA · Food and drugs·Recall number Z-2253-2024
BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
Published July 17, 2024 · Recall initiated: June 12, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Sterilization certificates could not be validated by the supplier
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Synergetics Inc
- Distributor
- US Nationwide
- Lot
- UDI/DI 20841305107605, Lot Number P62764965R
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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