Class III โ€” Low Risk

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

Metoprolol Tartrate Injection Recalled by RemedyRepack Inc. Due to Failed pH Specifications: High Out-of-Specification results for pH...

Date: October 26, 2018
Company: RemedyRepack Inc.
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 RemedyRepack Inc. directly.

Affected Products

Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902, NDC# 70518-0868-00

Quantity: 1 vial

Why Was This Recalled?

Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.

Where Was This Sold?

This product was distributed to 1 state: NY

Affected (1 state)Not affected

About RemedyRepack Inc.

RemedyRepack Inc. has 60 total recalls tracked by RecallDetector.

Related Recalls

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