Regenerative Processing Plant recalls LITE Regener-Eyes ophthalmic solution (glycerin 0.4%) due to lack of sterility assurance. Products with specific lot numbers and expiration dates are affected. Consumers should check their product details and contact the manufacturer for guidance.
Lack of Sterility Assurance
Regenerative Processing Plant is recalling LITE Regener-Eyes ophthalmic solution (glycerin 0.4%) bottles because they may not be sterile. This could cause infections if used improperly. The recall affects specific lot numbers and expiration dates.
The product may not be sterile, which can lead to infections if used in the eyes. Ophthalmic solutions are meant for direct application to the eye, so contamination could cause serious eye infections.
People who have purchased LITE Regener-Eyes ophthalmic solution (glycerin 0.4%) bottles with the listed lot numbers and expiration dates are affected. Those using the product for eye care are at risk of infection if the solution is not sterile.
Check the product label for the lot numbers listed (e.g., P121322A, P121422A) and expiration dates (e.g., 12/13/2024). The product is a 3mL bottle of ophthalmic solution with glycerin 0.4%.
Look for the lot numbers and expiration dates on the bottle label to determine if it is part of the recall.
The recall states there is a lack of sterility assurance, so the product may not be safe for eye use and could cause infections. Do not use the product until you confirm it is not recalled.
Check the lot numbers and expiration dates on the bottle label. The affected products include specific lot numbers like P121322A (exp. 12/13/2024) and others listed in the recall notice.
The recall does not specify a remedy, so contact the manufacturer directly for guidance on what to do with the product.
We’ve drafted a message you can send Regenerative Processing Plant to request your refund or repair — edit it as you like.
Subject: Recall D-0152-2025 — Regenerative Processing Plant Regenerative Processing Plant Hello, I own a Regenerative Processing Plant that is covered by recall D-0152-2025 from Regenerative Processing Plant. 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.
