# FDA recall D-0600-2024

> **Zydus Pharmaceuticals (USA) Inc** · Class II · drug recall initiated 2024-06-27.

## Product

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

## Distribution

TN

## Key facts

- **Recall number:** D-0600-2024
- **Recalling firm:** Zydus Pharmaceuticals (USA) Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-06-27
- **Report date:** 2024-07-24
- **Termination date:** 2025-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Pennington, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0600-2024

## Citation

> AI Analytics. FDA recall D-0600-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0600-2024. Source: US FDA. Licensed CC0.

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