Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ED Mix Injections Recalled by FVS Holdings, Inc. dba. Green Valley Drugs Due to Lack of Assurance of Sterility: all sterile products...
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 FVS Holdings, Inc. dba. Green Valley Drugs directly.
Affected Products
ED Mix Injections, all strengths and all presentations including a) ED mix TM -at 2, b) ED-Mix BI-Mix 10 30 mL, c) ED-Mix BI-Mix 9 30 mL; d) ED-Mix BI-Mix-3-30, e) ED-Mix PGE 80-30, f) ED-Mix SB4 30 mL, g) Ed-Mix ST 9E, h) ED-Mix ST-1, i) ED-MIX T106, j) ED-MIX-PGE-150 30 mL, k) ED-MIX-PGE-40-30, l) ED-MIX-ST 9A, m) ED-MIX-ST 9D, n) ED-MIX-ST-9B, o) ED-MIX-T 101, p) ED-MIX-T105, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Quantity: 10684 vials
Why Was This Recalled?
Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About FVS Holdings, Inc. dba. Green Valley Drugs
FVS Holdings, Inc. dba. Green Valley Drugs has 78 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report