Global Pharma Healthcare is recalling artificial tears eye drops manufactured in the same facility with contamination issues. These products may contain harmful substances due to CGMP deviations.
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be contaminated.
Global Pharma Healthcare is recalling certain lubricant eye drops that were manufactured in the same facility as contaminated batches. This recall is due to potential contamination from CGMP deviations during production.
The eye drops were produced in the same facility as batches found to be contaminated. CGMP deviations indicate possible contamination during manufacturing, which could lead to harmful substances entering the eye.
People who purchased the recalled eye drops from the listed lots and expiration dates are affected. Those with sensitive eyes or allergies may be at higher risk.
Check the product label for the lot numbers PCMH009 through PCMI008 and expiration dates listed (Nov-2023 to MAR-2025). The product is distributed by EzriCare, LLC in Lakewood, NJ.
Look for lot numbers PCMH009 through PCMI008 and expiration dates from Nov-2023 to MAR-2025 on the bottle.
The recall is due to CGMP deviations in manufacturing, which means the eye drops were produced in the same facility as contaminated batches.
The official notice does not specify a remedy for this recall, so contact the manufacturer for further instructions.
The recall notice does not mention specific risks for certain users, but people with sensitive eyes or allergies may be at higher risk.
We’ve drafted a message you can send Global Pharma Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0920-2023 — Global Pharma Healthcare Global Pharma Healthcare Hello, I own a Global Pharma Healthcare that is covered by recall D-0920-2023 from Global Pharma 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.
