# FDA recall F-0814-2014

> **National Enzyme Co** · Class II · food recall initiated 2013-10-30.

## Product

Dietary Supplements packaged in the following configurations:   (1) Bulk Isolase-I powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 71453);  (2) Bulk Bision Isolase powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 72073);  (3) Bulk Isolase (Shanghai) powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 72077);  (4) Bulk Isolase (Wedar) powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 72080);  (5) Bulk Isolase (Nutri Sport) powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for intern

## Reason for recall

Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol

## Distribution

Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.

## Key facts

- **Recall number:** F-0814-2014
- **Recalling firm:** National Enzyme Co
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2013-10-30
- **Report date:** 2013-12-25
- **Termination date:** 2015-03-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Forsyth, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0814-2014

## Citation

> AI Analytics. FDA recall F-0814-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/F-0814-2014. Source: US FDA. Licensed CC0.

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