# FDA recall D-0740-2021

> **Teva Pharmaceuticals USA** · Class II · drug recall initiated 2021-07-29.

## Product

Adenosine Injection, USP, 60mg/20mL (3 mg/mL), 20 mL single-dose vial, Rx only, Manufactured by: Teva Pharmaceuticals USA Inc. Parsippany, NJ 07054, NDC 0703-8776-01

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Product was distributed Nationwide, including Puerto Rico.

## Key facts

- **Recall number:** D-0740-2021
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-07-29
- **Report date:** 2021-08-25
- **Termination date:** 2024-06-04

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0740-2021

## Citation

> AI Analytics. FDA recall D-0740-2021. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/D-0740-2021. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*