PlainRecalls
FDA Drug Moderate Class II Terminated

Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose Vial, For Intravenous Use Only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 Made in India NDC 55150-307-01

Reported: February 10, 2021 Initiated: December 30, 2020 #D-0248-2021

Product Description

Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose Vial, For Intravenous Use Only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 Made in India NDC 55150-307-01

Reason for Recall

Discoloration and failed pH specifications

Details

Recalling Firm
AuroMedics Pharma LLC
Units Affected
3094 cartons
Distribution
Nationwide
Location
East Windsor, NJ

Frequently Asked Questions

What product was recalled?
Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose Vial, For Intravenous Use Only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 Made in India NDC 55150-307-01. Recalled by AuroMedics Pharma LLC. Units affected: 3094 cartons.
Why was this product recalled?
Discoloration and failed pH specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on February 10, 2021. Severity: Moderate. Recall number: D-0248-2021.