Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride Recalled by SCA Pharmaceuticals, LLC Due to Lack Of Assurance Of Sterility.

Date: October 19, 2017
Company: SCA Pharmaceuticals, LLC
Status: Terminated
Source: FDA (Drug)

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 SCA Pharmaceuticals, LLC directly.

Affected Products

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

Quantity: 128 syringes

Why Was This Recalled?

Lack Of Assurance Of Sterility.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About SCA Pharmaceuticals, LLC

SCA Pharmaceuticals, LLC has 56 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report