Shilpa Medicare recalls PEMRYDI RTU (pemetrexed injection) vials with green discoloration. This may indicate contamination and should be discarded to avoid potential health risks.
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Shilpa Medicare is recalling PEMRYDI RTU (pemetrexed injection) vials that have turned green. This discoloration could indicate contamination, so affected users should stop using the product and contact their healthcare provider.
The vials may have become contaminated due to discoloration turning green. While the exact risk is not specified, discoloration in medical injections can indicate potential contamination that might cause health issues.
Patients prescribed PEMRYDI RTU injections by a healthcare provider. Those with green discoloration in the vial are most at risk.
Check for green to dark green discoloration in the vial. The product is a single-dose injection vial labeled PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL, manufactured by Zydus Lifesciences Limited.
Discard the vial immediately if it shows green to dark green discoloration.
The recall only applies to vials with green to dark green discoloration. If the vial is clear, it may be safe to use as per the prescription.
Look for green to dark green discoloration in the vial. The product is a single-dose injection vial labeled PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL, manufactured by Zydus Lifesciences Limited.
Discard the vial immediately and contact your healthcare provider for further instructions.
We’ve drafted a message you can send Shilpa Medicare to request your refund or repair — edit it as you like.
Subject: Recall D-0764-2026 — Shilpa Medicare Shilpa Medicare Hello, I own a Shilpa Medicare that is covered by recall D-0764-2026 from Shilpa Medicare. 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.
