FarmaKeio recalls BPC-157 2mg/mL injections due to potential sterility issues. This affects sterile medical products made under questionable manufacturing practices.
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
FarmaKeio is recalling BPC-157 2 mg/mL (5 mL) injections because they may not be sterile. This is a serious risk for patients using these injections under a prescription.
The product was made under manufacturing practices that could compromise sterility. This means the injections might contain harmful bacteria or other contaminants, which can cause serious infections or illness if used.
Prescription patients using BPC-157 injections from Farmakeio. Those with the specific lot numbers listed in the recall are most at risk.
Check the vial label for the product name 'BPC-157 2 mg/mL (5 mL) Injection'. Look for lot numbers 32242 (BUD: 4/19/2022) or 33911 (BUD: 6/8/2022).
Immediately discard any BPC-157 injections with lot numbers 32242 or 33911.
No, the product may not be sterile and could cause serious infections. Do not use these injections.
Discard the product immediately and contact Farmakeio for further instructions.
Look for lot numbers 32242 (BUD: 4/19/2022) or 33911 (BUD: 6/8/2022) on the vial label.
We’ve drafted a message you can send FarmaKeio to request your refund or repair — edit it as you like.
Subject: Recall D-0776-2022 — FarmaKeio FarmaKeio Hello, I own a FarmaKeio that is covered by recall D-0776-2022 from FarmaKeio. 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.
