Jubilant Cadista recalls 4mg methylprednisolone tablets due to subpotent content. This may affect medication effectiveness. Check NDC 59746-0:001-06 or lot #21P0322 for affected products.
Subpotent
Jubilant Cadista is recalling 4mg methylprednisolone tablets that may not contain enough active ingredient. This could lead to ineffective treatment if used for medical conditions requiring precise dosing.
The tablets may have lower-than-stated potency, meaning they might not provide the intended medical effect. This could result in inadequate treatment for conditions like inflammation or autoimmune disorders.
People prescribed methylprednisolone tablets by a doctor who received this specific product. Those with conditions requiring precise steroid dosing are most at risk.
Check for the NDC code 59746-001-06 or lot number 21P0322 on the product packaging. The product is a 100-count bottle sold by prescription only.
Look for the NDC code 59746-001-06 or lot number 21P0322 on the bottle.
The recall is for potential subpotency, which may affect effectiveness but does not indicate immediate safety risks. Consult your doctor for guidance.
Check the NDC code 59746-001-06 or lot number 21P0322 on the product packaging.
The recall does not specify a remedy, so contact your doctor to discuss whether to continue using the product.
We’ve drafted a message you can send Jubilant Cadista to request your refund or repair — edit it as you like.
Subject: Recall D-0752-2022 — Jubilant Cadista Jubilant Cadista Hello, I own a Jubilant Cadista that is covered by recall D-0752-2022 from Jubilant Cadista. 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.
