# FDA recall D-0001-2015

> **Cubist Pharmaceuticals, Inc.** · Class I · drug recall initiated 2014-08-01.

## Product

CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for: Cubist Pharmaceuticals, Inc., Lexington, MA 02421, NDC 67919-011-01, UPC 3 67919-011-01 6.

## Reason for recall

Presence of Particulate Matter: Potential presence of glass particulate matter in the vials.

## Distribution

Nationwide   Foreign:  Israel, Taiwan

## Key facts

- **Recall number:** D-0001-2015
- **Recalling firm:** Cubist Pharmaceuticals, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-08-01
- **Report date:** 2014-10-08
- **Termination date:** 2016-06-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lexington, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0001-2015

## Citation

> AI Analytics. FDA recall D-0001-2015. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0001-2015. Source: US FDA. Licensed CC0.

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