Preferred Pharmaceuticals is recalling 15mg Lansoprazole Delayed-Release Capsules (90-count) after stability testing showed dissolution problems. This may affect drug effectiveness.
Out of specification results observed in dissolution during long term stability testing.
Preferred Pharmaceuticals is recalling 15mg Lansoprazole Delayed-Release Capsules (90-count) because stability testing found dissolution issues. This could mean the medication doesn't work as intended.
The recall is based on stability testing showing dissolution problems. This means the medication might not release the active ingredient properly over time, potentially reducing its effectiveness.
People who purchased the 15mg Lansoprazole Delayed-Release Capsules (90-count) from Dr Reddy's Laboratories Limited. Those with acid reflux conditions are most at risk if the medication doesn't work properly.
Check for the 90-count bottle labeled 'Lansoprazole Delayed-Release Capsules, 15mg' with NDC 68788-6390-09. The product was sold by Dr Reddy's Laboratories Limited with specific lot numbers and expiration date 12/31/2023.
Look for the NDC code 68788-6390-09 on the bottle label to confirm if it's recalled.
The recall is due to dissolution testing showing issues that could affect the medication's effectiveness.
The recall is for potential reduced effectiveness, not a safety hazard causing injury.
Check for the NDC code 68788-6390-09 on the bottle label, which was sold by Dr Reddy's Laboratories Limited with specific lot numbers and expiration date 12/31/2023.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0769-2022 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0769-2022 from Preferred 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.
