New England Compounding Center recalls all non-sterile products made by their facility in Framingham, MA due to GMP deviations. Consumers should check product lot codes for affected items.
GMP Deviations
New England Compounding Center has recalled all non-sterile products made at their Framingham, MA facility because of manufacturing quality control issues. This recall is due to deviations in Good Manufacturing Practices that could affect product safety.
The recall is due to GMP deviations, which means the products may not meet the required quality standards for safety and effectiveness. This could lead to potential health risks if the products are used without proper quality control.
Anyone who has purchased non-sterile products from New England Compounding Center's facility in Framingham, MA. People who use these products for medical purposes are most at risk.
Check the product label for the manufacturer name 'New England Compounding Center' and the lot code. Products were sold online and through pharmacies in the United States starting from when the recall was announced.
Look for the manufacturer name 'New England Compounding Center' and the lot code on the product label.
The recall is due to GMP deviations, which means the products may not meet the required quality standards for safety and effectiveness.
Check the product label for the manufacturer name 'New England Compounding Center' and the lot code.
The official notice does not specify a remedy for this recall.
We’ve drafted a message you can send New England Compounding Center to request your refund or repair — edit it as you like.
Subject: Recall D-053-2013 — New England Compounding Center New England Compounding Center Hello, I own a New England Compounding Center that is covered by recall D-053-2013 from New England Compounding Center. 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.
