The Recall Desk
CriticalFDA (Drugs)·D-0928-2019·Announced 2019-03-20

King Bio Inc. Recalls NET Remedies #11 Homeopathic Preparation Due to Microbial Contamination

King Bio Inc. is recalling NET Remedies #11 Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

What this means for you

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The FDA has classified this recall as Class I, which per the rubric mandates a severity score of 5 (Critical) regardless of other factors.

Plain-English summary

King Bio Inc. is recalling NET Remedies #11 (Lilac Label) Homeopathic Preparation, Oral Liquid, 57 mL, due to microbial contamination. The recalled product was manufactured by King Bio Inc. U.S.A. and supplied by NET (Australia) Pty LTD. The recall involves 599 bottles with lot numbers AUS-072018C (Exp. 07/20) and AUS-100117D (Exp. 10/19).

The product was distributed nationwide in the U.S.A., as well as in Canada and Australia. The FDA has classified this recall as Class I, which is the most serious type of recall, indicating a reasonable probability that the use of, or exposure to, the violative product will cause serious adverse health consequences or death.

Consumers who have purchased this product should stop using it and contact King Bio Inc. for further instructions on how to return the product or obtain a refund.

The recalled product

Product
NET Remedies #11 (Lilac Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic Preparation
Hazard
Affected units
599

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 (2)

  • Lots: AUS-072018C Exp. 07/20
  • AUS-100117D Exp. 10/19

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 465 recalled by King Bio Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 465 products in this recall →

Related recalls

Same manufacturer · King Bio Inc.

See all →

Same hazard · microbial contamination

See all →