Regenerative Processing Plant recalls 3mL glycerin 0.5% ophthalmic solution due to lack of sterility assurance. Affected lots have specific expiration dates and may cause infection if used.
Lack of Sterility Assurance
Regenerative Processing Plant is recalling 3mL bottles of Regener-Eyes ophthalmic solution (glycerin 0.5%) because they lack sterility assurance. This could lead to eye infections if used improperly.
The ophthalmic solution lacks proper sterility assurance, meaning it may contain contaminants that could cause eye infections. This is a risk during medical use, especially for sensitive eye conditions.
People who use this eye solution for medical purposes, especially those with compromised immune systems or open wounds. The risk is low but could cause infection if the product is not sterile.
Check the product label for the name 'Regener-Eyes', 3mL bottles, and the lot numbers listed in the recall (e.g., P120522A, P120522B, etc.). The expiration dates range from December 2024 to May 2025.
Look for the lot numbers listed in the recall (e.g., P120522A, P120522B) and expiration dates from December 2024 to May 2025.
If you cannot confirm the lot number or expiration date, discard the product to avoid potential infection risks.
Regener-Eyes ophthalmic solution (glycerin 0.5%), 3mL bottles with lot numbers from P120522A to P022823A.
Check the product label for lot numbers listed in the recall (e.g., P120522A, P120522B) and expiration dates from December 2024 to May 2025.
The recall record does not specify a remedy, so users should check the product label and discard if unsure.
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-0153-2025 — Regenerative Processing Plant Regenerative Processing Plant Hello, I own a Regenerative Processing Plant that is covered by recall D-0153-2025 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.
