Major Pharmaceuticals recalls Potassium Chloride Extended-Release Tablets due to failed dissolution specifications. This could affect medication effectiveness. Check your product details and contact the manufacturer for instructions.
Failed Dissolution Specifications.
Major Pharmaceuticals is recalling Potassium Chloride Extended-Release Tablets because they failed dissolution specifications. This means the tablets may not release potassium chloride properly, potentially affecting medication effectiveness. Consumers should check their product details and contact the manufacturer for instructions.
The tablets failed dissolution specifications, meaning they may not release potassium chloride as intended. This could lead to improper medication effectiveness. The exact risk level is not clearly described in the recall notice.
People who have the Potassium Chloride Extended-Release Tablets (10 mEq/750 mg) with NDC 0904-7216-61 and lot number T05224 are affected. Those using these tablets for medical purposes are most at risk.
Check for the product name 'Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters)'. Look for NDC 0904-7216-61 and lot number T05224 on the packaging.
Look for NDC 0904-7216-61 and lot number T05224 on the packaging to confirm if your product is recalled.
The recall states the tablets failed dissolution specifications, but the exact risk level is not clearly described. The manufacturer does not specify if the product is safe to use.
The recall does not provide specific remedy steps. Check product details and contact the manufacturer for instructions.
Check for NDC 0904-7216-61 and lot number T05224 on the packaging. The manufacturer does not provide additional details on how to confirm the recall.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0221-2025 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0221-2025 from Major Pharmaceuticals. 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.
