Kilitch Healthcare India Limited recalls Multi-action Relief Drops due to non-sterility. All lots of 0.5 fl oz bottles distributed by Rite Aid are affected. Consumers should contact the manufacturer for details.
Non-Sterility
Kilitch Healthcare India Limited is recalling Multi-action Relief Drops because they may not be sterile. This could pose a risk of infection if used. All lots of the product are affected.
The product may not be sterile, which could lead to infections if the drops are used. This is a non-sterility issue, meaning the product might not meet safety standards for medical use.
People who own or use the Multi-action Relief Drops (0.5 fl oz bottles) distributed by Rite Aid are affected. Those with sensitive eyes or open wounds may be at higher risk.
Check for Multi-action Relief Drops in 0.5 fl oz (15 mL) bottles with the NDC number 11822-2254-3. The product was distributed by Rite Aid in the US.
Reach out to Kilitch Healthcare India Limited for specific instructions on handling the recalled product.
The recall states the product may not be sterile, so it is not safe to use as it could cause infections.
Look for Multi-action Relief Drops in 0.5 fl oz (15 mL) bottles with NDC 11822-2254-3 distributed by Rite Aid.
Contact Kilitch Healthcare India Limited for specific instructions on handling the recalled product.
We’ve drafted a message you can send Kilitch Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0308-2024 — Kilitch Healthcare Kilitch Healthcare Hello, I own a Kilitch Healthcare that is covered by recall D-0308-2024 from Kilitch Healthcare. 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.
