Synergetics Inc recalls BAUSCH+LOMB I-PACK Injection Kit REF 18060 due to unverified sterilization certificates. This affects intravitreal eye injections. Contact for details.
Sterilization certificates could not be validated by the supplier
Synergetics Inc has recalled BAUSCH+LOMB I-PACK Injection Kit REF 18060 for intravitreal eye injections because sterilization certificates could not be validated by the supplier. This means the product may not be sterile, posing a risk of infection during eye procedures.
Sterilization certificates are critical for ensuring the kit is sterile before use. If these certificates cannot be validated by the supplier, the kit may not be sterile, increasing the risk of infection during eye injections.
Patients receiving intravitreal eye injections using this specific kit are most at risk. The recall applies to kits with the UDI/DI 20841305107544 and Lot Number P62764979R.
Check for the UDI/DI number 20841305107544 and Lot Number P62764979R on the kit. This product is used for intravitreal eye injections and was sold by Synergetics Inc.
Verify the UDI/DI number 20841305107544 and Lot Number P62764979R on the kit.
Sterilization certificates could not be validated by the supplier, which may mean the kit is not sterile.
Look for the UDI/DI number 20841305107544 and Lot Number P62764979R on the kit.
The recall record does not specify a remedy, so contact Synergetics Inc for further instructions.
We’ve drafted a message you can send BAUSCH+LOMB to request your refund or repair — edit it as you like.
Subject: Recall Z-2251-2024 — BAUSCH+LOMB BAUSCH+LOMB Hello, I own a BAUSCH+LOMB that is covered by recall Z-2251-2024 from BAUSCH+LOMB. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
