Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HYDROmorphone 20 mg/100 mL Injectable Solution Recalled by Advanced Pharma Inc. Due to Sub-potency
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 Advanced Pharma Inc. directly.
Affected Products
HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10
Quantity: 560 bags
Why Was This Recalled?
Sub-potency
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Advanced Pharma Inc.
Advanced Pharma Inc. has 99 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report