Jubilant Cadista recalls Meclizine Hydrochloride Tablets with incorrect Prednisone labeling. This mix-up could lead to wrong medication use. Consumers should check labels and contact the manufacturer for details.
Labeling: Label mix-up: Incorrect label placed on product. Shipper cases labeled Meclizine Hydrochloride Tablets contain bottles incorrectly labeled as PredniSONE Tablets. The tablets in the bottles are Meclizine Hydrochloride
Jubilant Cadista is recalling Meclizine Hydrochloride Tablets that have been incorrectly labeled as Prednisone. This mix-up could cause someone to take the wrong medication, which might lead to health risks.
The tablets are labeled incorrectly as Prednisone, a different medication. This mix-up could lead to someone taking the wrong medication, which might cause health issues if they are not supposed to take Prednisone.
People who have Meclizine Hydrochloride Tablets labeled as Prednisone. Those with prescription medications for conditions like allergies or vertigo are most at risk.
Check for Meclizine Hydrochloride Tablets labeled as Prednisone. The product was sold in cases of 24 bottles (100-count bottle) with NDC 59746-122-06, manufactured in Salisbury, MD, Lot # 22P0036, expiring 12/2024.
Look for Meclizine Hydrochloride Tablets labeled as Prednisone. If found, do not use them.
The product is not safe to use as it has been incorrectly labeled. Do not use if labeled as Prednisone.
Check for Meclizine Hydrochloride Tablets labeled as Prednisone. The product was sold in cases of 24 bottles (100-count bottle) with NDC 59746-122-06, manufactured in Salisbury, MD, Lot # 22P0036, expiring 12/2024.
Do not use the product if labeled as Prednisone. Contact Jubilant Cadista Pharmaceuticals for further instructions.
We’ve drafted a message you can send Jubilant Cadista to request your refund or repair — edit it as you like.
Subject: Recall D-0767-2022 — Jubilant Cadista Jubilant Cadista Hello, I own a Jubilant Cadista that is covered by recall D-0767-2022 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.
