# FDA recall D-885-2013

> **Bracco Diagnostics Inc** · Class II · drug recall initiated 2013-06-21.

## Product

Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution), USP, 37% Organically Bound Iodine, 120 ml bottle, Rx only, Manufactured for Bracco Diagnostics Inc. Princeton, NJ 08543  by Therapex, Division of E-Z-EM Canada Inc. Anjou Quebec H1J2Z4, Canada, NDC 0270-0445-40

## Reason for recall

Presence of foreign substance: One lot of the product may contain black foreign particles

## Distribution

Nationwide

## Key facts

- **Recall number:** D-885-2013
- **Recalling firm:** Bracco Diagnostics Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-06-21
- **Report date:** 2013-08-21
- **Termination date:** 2015-01-23

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-885-2013

## Citation

> AI Analytics. FDA recall D-885-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-885-2013. Source: US FDA. Licensed CC0.

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