Synergetics Inc recalls BAUSCH+LOMB I-PACK Injection Kit with Drape REF 18061 due to unvalidated sterilization certificates. This affects intravitreal injection kits sold with UDI/DI 20841305107551 and Lot P63044983R.
Sterilization certificates could not be validated by the supplier
Synergetics Inc recalls BAUSCH+LOMB I-PACK Injection Kits with Drape (REF 18061) for intravitreal eye injections. The recall is because sterilization certificates could not be validated by the supplier, which may lead to infection risks.
Sterilization certificates are required to ensure the kit is safe for medical use. If these certificates cannot be validated, the kit might not be sterile, increasing the risk of infection during eye injections.
Eye care professionals who use this kit for intravitreal injections are affected. Patients receiving injections with this specific kit may be at risk of infection.
Check for the product name 'BAUSCH+LOMB I-PACK Injection Kit with Drape', reference number REF 18061, and the unique identifier UDI/DI 20841305107551 with lot number P63044983R.
Look for the reference number REF 18061 and unique identifier UDI/DI 20841305107551 with lot number P63044983R.
Sterilization certificates could not be validated by the supplier, which may lead to infection risks during eye injections.
Check for the product name 'BAUSCH+LOMB I-PACK Injection Kit with Drape', reference number REF 18061, and the unique identifier UDI/DI 20841305107551 with lot number P63044983R.
The recall record does not specify a remedy, so contact the manufacturer for guidance.
We’ve drafted a message you can send BAUSCH+LOMB to request your refund or repair — edit it as you like.
Subject: Recall Z-2252-2024 — BAUSCH+LOMB BAUSCH+LOMB Hello, I own a BAUSCH+LOMB that is covered by recall Z-2252-2024 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.
