Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Hydromorphone HCl in 0.9% sodium chloride Recalled by PharMEDium Services, LLC Due to Incorrect Product Formulation; Firm's customer resource center (CRC)...

Date: June 7, 2019
Company: PharMEDium Services, 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 PharMEDium Services, LLC directly.

Affected Products

Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD Syringe, PharMEDium 913 N Davis Ave Cleveland, MS 38732, 800-523-7749, NDC 61553-352-78

Quantity: 28,140 syringes

Why Was This Recalled?

Incorrect Product Formulation; Firm's customer resource center (CRC) statement indicates that the product is sulfite free, however the product is produced with a raw material that contains sulfite

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About PharMEDium Services, LLC

PharMEDium Services, LLC has 21 total recalls tracked by RecallDetector.

Related Recalls

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