BAUSCH+LO: I-PACK Injection Kit Custom Recall for Sterilization Issues

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Recalling firmSynergetics Inc3845 Corporate Centre Dr, N/A · O Fallon, MO 63368-8678

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✎ GovInfoNow plain-language explainer

What happened, in plain English

BAUSCH+LOMB's I-PACK Injection Kit Custom (REF 18069) is recalled because supplier sterilization certificates couldn't be validated. This could lead to infection risks during eye injections if used without proper sterilization.

Why it’s dangerous

The supplier's sterilization certificates for the injection kit couldn't be validated, meaning the kit might not be properly sterilized. This could lead to infection risks during eye injections if the kit is used without proper sterilization.

Who’s affected

Eye care professionals using the I-PACK Injection Kit Custom (REF 18069) for intravitreal injections. Those who have the specific lot number P62764965R are most at risk.

How to tell if you have this one

Check for the product name 'I-PACK Injection Kit Custom', reference number REF 18069, and lot number P62764965R. The kit is used for intravitreal eye injections.

Brand
BAUSCH+LOMB
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Sterilization Certificates
Verify if the kit has valid sterilization certificates from the supplier before use.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The supplier's sterilization certificates for the injection kit couldn't be validated, which may lead to infection risks during eye injections.

What should I do if I have this product?

Check if you have the I-PACK Injection Kit Custom (REF 18069) with lot number P62764965R. If so, verify sterilization certificates before use.

Is there a risk of serious injury?

The recall is due to potential infection risks from unverified sterilization, not immediate serious injury risks.

Take action

Contact BAUSCH+LOMB

We’ve drafted a message you can send BAUSCH+LOMB to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2253-2024 — BAUSCH+LOMB BAUSCH+LOMB

Hello,

I own a BAUSCH+LOMB that is covered by recall Z-2253-2024 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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Where this comes from

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.

Official source: FDA Recall #Z-2253-2024 (June 12, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2253-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)

Lower-risk recall