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 Recalled by Sentara Enterprises Due to Lack of Assurance of Sterility: Product sterility cannot...

Date: September 18, 2015
Company: Sentara Enterprises
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 Sentara Enterprises directly.

Affected Products

HYDROMORPHONE HCL, Packaged as a) 2.5MG in 1ML Syringes, b) 150MG in 75ML Homepumps, c) 125MG in 125ML Homepumps, d) 250MG in 125ML Homepumps, e) 135MG in 135ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.

Quantity: a) 42 Syringes, b) 6 Bags, c) 4 Bags, d) 4 Bags, e) 1 Bag

Why Was This Recalled?

Lack of Assurance of Sterility: Product sterility cannot be guaranteed.

Where Was This Sold?

This product was distributed to 2 states: NC, VA

Affected (2 states)Not affected

About Sentara Enterprises

Sentara Enterprises has 34 total recalls tracked by RecallDetector.

Related Recalls

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