Strides Pharma recalls 20mg Prednisone tablets with foreign 2.5mg tablets. Consumers should check NDC 64380-785-06 and lot 7248988B for affected products.
Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets
Strides Pharma is recalling Prednisone Tablets (20mg, 100-count) due to foreign tablets (2.5mg) in the product. This could cause incorrect dosing if taken without knowing the extra tablet.
The product contains a foreign 2.5mg tablet that could be mistaken for a regular tablet. This may lead to incorrect dosing if the user takes the tablet without realizing the extra tablet is present.
Prescription holders of Prednisone Tablets 20mg, 10:00-count bottles with NDC 64380-785-06 and lot 7248988B. People taking this medication for conditions like arthritis or asthma are most at risk.
Check for NDC 64380-785-06 and lot number 7248988B on the bottle. The product is sold as a 100-count bottle of Prednisone Tablets 20mg, Rx Only.
Look for NDC 64380-785-06 and lot number 7248988B on the bottle.
The recall is for a foreign tablet that could cause incorrect dosing, but the risk is low as it's a prescription product.
Check for NDC 64380-785-06 and lot number 7248988B on the bottle.
The recall does not specify a remedy, so contact your doctor or pharmacist for advice.
We’ve drafted a message you can send Strides Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-1330-2022 — Strides Pharma Strides Pharma Hello, I own a Strides Pharma that is covered by recall D-1330-2022 from Strides Pharma. 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.
