BAUSCH+LOMB I-PACK Injection Kit with Wire Speculum (REF 18069W) recalled due to unverified sterilization certificates. This device is used for eye injections and may pose risks if not properly sterilized.
Sterilization certificates could not be validated by the supplier
BAUSCH+LOMB is recalling its I-PACK Injection Kit with Wire Speculum (REF 18069W) because sterilization certificates could not be validated by the supplier. This means the kit might not be properly sterilized, which could lead to infections during eye injections.
Sterilization certificates are critical for ensuring the kit is safe for medical use. If these certificates cannot be validated, the kit might not be properly sterilized, increasing the risk of infection during eye injections.
Eye care professionals who use this kit for intravitreal injections are most at risk. Patients receiving injections with this kit could be affected if the sterilization is compromised.
Check for the product name 'I-PACK Injection Kit with Wire Speculum', reference number REF 18069W, and lot number P62764970R. This kit is used for intravitreal eye injections.
Verify if the kit has valid sterilization certificates from the supplier.
The recall states that sterilization certificates could not be validated by the supplier, so the product may not be safe for use.
The recall does not specify a remedy, so there is no action required beyond checking sterilization certificates.
Look for the product name 'I-PACK Injection Kit with Wire Speculum', reference number REF 18069W, and lot number P62764970R.
We’ve drafted a message you can send BAUSCH+LOMB to request your refund or repair — edit it as you like.
Subject: Recall Z-2254-2024 — BAUSCH+LOMB BAUSCH+LOMB Hello, I own a BAUSCH+LOMB that is covered by recall Z-2254-2024 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.
