Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LL-37 2 mg/mL (5 mL) Injection Recalled by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding Due to Lack of Assurance of Sterility: deviations from Current...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding directly.
Affected Products
LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
Quantity: 25 vials
Why Was This Recalled?
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report