BLI International recalls 4 mg Chlorpheniramine tablets (NDC 53185-277-24) manufactured for Athlete's Needs. Stability failure risks inaccurate dosing after 6 months.
Superpotent Drug: Stability failure for assay at 6 months test time-point.
BLI International is recalling 4 mg Chlorpheniramine Maleate tablets in 24-count bottles that were manufactured for Athlete's Needs. The recall is due to stability issues that could lead to inaccurate dosing after 6 months.
The tablets may lose potency or become unstable after 6 months of storage, potentially leading to inaccurate dosing. This could cause under-dosing if the medication becomes less effective over time.
People who purchased the 24-count Chlorpheniramine tablets from Athlete's Needs in Novi, MI. Those most at risk are individuals using the medication for allergies who may need precise dosing.
Check for the 24-count bottle labeled 'Chlorpheniramine Maleate 4 mg' manufactured for Athlete's Needs. Look for the lot number 24A27724 and expiration date 01/31/2027 on the packaging.
Verify the expiration date (01/31/2027) and lot number (24A27724) on the packaging.
The recall is for stability issues that could affect dosing accuracy after 6 months, but the product is safe if used before expiration.
The recall does not specify a remedy, so check the expiration date and lot number before using.
The stability test showed failure at 6 months, but the actual shelf life may vary.
We’ve drafted a message you can send BLI International to request your refund or repair — edit it as you like.
Subject: Recall D-0029-2025 — BLI International BLI International Hello, I own a BLI International that is covered by recall D-0029-2025 from BLI International. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.