Global Corporation recalls Broncochem Cold & Tea (acetaminophen, phenylephrine, HCl, chlorpheniramine maleate) due to stability failures in some ingredients. Products with specific lot numbers and expiration dates are affected.
Stability testing failures for one or two of the four active pharmaceutical ingredients among the finished drug products, i.e., Phenylephrine HCL, and/or Chlorpheniramine Maleate.
Global Corporation is recalling Broncochem Cold & Tea sachets because stability testing showed issues with some ingredients. This could lead to ineffective medication if the product degrades over time.
Stability testing found that one or two of the four active ingredients (phenylephrine HCl and/or chlorpheniramine maleate) may degrade over time. This could result in the product becoming ineffective for treating cold symptoms.
People who purchased Broncochem Cold & Tea sachets with specific lot numbers and expiration dates from the Dominican Republic. Those using the product for cold symptoms are most at risk if the ingredients degrade.
Check the product label for lot numbers 123255, 123256 (expiring 11/2024) or 123637 (expiring 03/2025). The product is packaged in 13g sachets, 25 per box, made in the Dominican Republic.
Look for lot numbers 123255, 123256 (expiring 11/2024) or 123637 (expiring 03/2025) on the packaging.
Stability testing found issues with one or two of the four active ingredients, which could make the product ineffective over time.
Check the product label for the specific lot numbers mentioned. If you have the affected lot numbers, contact Global Corporation for further instructions.
The recall is for potential ineffectiveness, not a risk of serious injury. The danger level is low risk.
We’ve drafted a message you can send Global Corporation to request your refund or repair — edit it as you like.
Subject: Recall D-0387-2024 — Global Corporation Global Corporation Hello, I own a Global Corporation that is covered by recall D-0387-2024 from Global Corporation. 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.
