The Recall Desk
ModerateFDA (Food)·F-0809-2014·Announced 2013-12-25

National Enzyme Recalls ZoiVi Digestive Formula Powder Due to Chloramphenicol

National Enzyme Co is recalling ZoiVi Digestive Formula powder because it may contain chloramphenicol above 0.3 ppb.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

National Enzyme Co is voluntarily recalling Bulk C812 ZoiVi Digestive Formula powder (SKU 83438) because the raw material used in the product may contain more than 0.3 ppb of chloramphenicol. The recalled product is packaged in poly bags within corrugated boxes for domestic distribution or fiber drums for international distribution.

The recall involves 77.85 kg of powder from Lot # 83438000. Domestic distribution was nationwide with direct accounts in 27 states across all geographical regions. International distribution included direct accounts in Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.

Consumers who have purchased this product should stop using it and contact National Enzyme Co for further instructions.

The recalled product

Product
Bulk C812 ZoiVi Digestive Formula powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83438)
Manufacturer
National Enzyme Co

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot #: 83438000

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 81 recalled by National Enzyme Co under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 81 products in this recall →