Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Recalled by Pharmedium Services Llc Due to Labeling: Incorrect or Missing Lot and/or Exp Date

Date: February 15, 2017
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

Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13

Quantity: 21 I.V. pumps

Why Was This Recalled?

Labeling: Incorrect or Missing Lot and/or Exp Date

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 7 total recalls tracked by RecallDetector.

Related Recalls

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