PlainRecalls
FDA Drug Moderate Class II Terminated

Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India, NDC 16714-165-01.

Reported: July 24, 2024 Initiated: June 27, 2024 #D-0600-2024

Product Description

Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India, NDC 16714-165-01.

Reason for Recall

Presence of particulate matter: glass

Details

Units Affected
432250 vials
Distribution
TN
Location
Pennington, NJ

Frequently Asked Questions

What product was recalled?
Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India, NDC 16714-165-01.. Recalled by Zydus Pharmaceuticals (USA) Inc. Units affected: 432250 vials.
Why was this product recalled?
Presence of particulate matter: glass
Which agency issued this recall?
This recall was issued by the FDA Drug on July 24, 2024. Severity: Moderate. Recall number: D-0600-2024.