US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 19, 2017 (9 years ago)

HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack Of Assurance Of Sterility.

What was recalled

HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17

Recalling firm
SCA Pharmaceuticals, LLC
NDC code
70004-0303-17
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0060-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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