Preferred Pharmaceuticals recalls 30-tablet Motrin Ibuprofen 400mg bottles made by Dr. Reddy's Laboratories with potential impurities. Consumers should check lot numbers and contact the company for details.
Failed Impurities/Degradation Specifications - at 18-month Stability testing
Preferred Pharmaceuticals is recalling Motrin Ibuprofen 400mg tablets that may have impurities. This could pose a risk to health if taken as directed, though the specific danger isn't detailed in the recall.
The tablets failed stability testing at 18 months, suggesting possible impurities that could affect safety. However, the recall doesn't specify how these impurities might cause harm or what the exact risk level is.
People who own or use the recalled Motrin Ibuprofen tablets made by Dr. Reddy's Laboratories. Those with chronic pain conditions or frequent users may be at higher risk.
Check for the lot numbers B0223H (expires 5/31/2026) or C3023H (expires 9/30/2026) on the bottle. The product is a 30-tablet Motrin Ibuprofen 400mg bottle manufactured by Dr. Reddy's Laboratories.
Look for the lot numbers B0223H or C3023H on the bottle label.
The recall states the tablets failed stability testing but does not specify if they are safe to take. Consumers should check the lot numbers and contact Preferred Pharmaceuticals for details.
The recall does not provide a remedy, so consumers should check the lot numbers and contact Preferred Pharmaceuticals for instructions.
Check for lot numbers B0223H (expires 5/31/2026) or C3023H (expires 9/30/2026) on the bottle label.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0647-2024 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0647-2024 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.
