Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902, NDC# 70518-0868-00
Reported: November 21, 2018 Initiated: October 26, 2018 #D-0245-2019
Product Description
Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902, NDC# 70518-0868-00
Reason for Recall
Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.
Details
- Recalling Firm
- RemedyRepack Inc.
- Units Affected
- 1 vial
- Distribution
- 1 vial was distributed to a medical facility in Mayville, NY.
- Location
- Indiana, PA
Frequently Asked Questions
What product was recalled? ▼
Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902, NDC# 70518-0868-00. Recalled by RemedyRepack Inc.. Units affected: 1 vial.
Why was this product recalled? ▼
Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 21, 2018. Severity: Low. Recall number: D-0245-2019.
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