Lacrimedics recalls specific collagen plug models due to potential pouch seal issues that could compromise sterility. Affected products include CP3, CP4, and CP5 dry eye treatments with certain lot numbers.
The sterile pouch seal may contain channels that could affect the seal integrity and potentially compromise sterility.
Lacrimedics is recalling specific collagen plug models (CP3, CP4, CP5) for dry eye treatment. The recall is due to a potential issue with the sterile pouch seal that could compromise sterility, meaning the products might not be safe for use.
The sterile pouch seal may have channels that could affect the seal integrity. This might compromise the sterility of the product, potentially leading to contamination if used.
People who have purchased the specific collagen plug models (CP3, CP4, CP5) for dry eye treatment from the listed lot numbers are affected. Those using these products for medical treatment are most at risk.
Check the product label for the model number (CP3, CP4, or CP5) and the lot number listed in the recall notice. The products are for dry eye treatment and require a prescription.
Look for the model number (CP3, CP4, or CP5) and lot number on the product packaging.
The sterile pouch seal may contain channels that could affect seal integrity and potentially compromise sterility.
CP3, CP4, and CP5 collagen plugs with specific lot numbers listed in the recall notice.
The recall does not specify a stop-use instruction; the remedy is null, so users can continue using but should check the product label for affected lots.
We’ve drafted a message you can send Lacrimedics to request your refund or repair — edit it as you like.
Subject: Recall Z-0709-2022 — Lacrimedics Lacrimedics Hello, I own a Lacrimedics that is covered by recall Z-0709-2022 from Lacrimedics. 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.
