# FDA recall D-0149-2021

> **BASF Corporation** · Class II · drug recall initiated 2020-11-17.

## Product

Kollidon CL-M Crospovidone Ph.Eur.Type B, USP/NF, JP, micronized, packaged in 30 kg plastic drums, Manufacturer: BASF SE, Carl-Bosch-Strabe 38, 67056 Ludwigshafen, Germany, Co-Manufactured by Siegfried PharmaChemikalien Minden GmbH, D-32423 Minden

## Reason for recall

Cross contamination: the excipient was found to be contaminated with theophylline.

## Distribution

USA Nationwide and Worldwide

## Key facts

- **Recall number:** D-0149-2021
- **Recalling firm:** BASF Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Completed
- **Initiation date:** 2020-11-17
- **Report date:** 2020-12-23

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0149-2021

## Citation

> AI Analytics. FDA recall D-0149-2021. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0149-2021. Source: US FDA. Licensed CC0.

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