The Recall Desk
Agency classClass IOur severity:CriticalFDA (Drugs)·D-0933-2019·Announced 2019-03-20

King Bio Homeopathic Liquid Recalled for Microbial Contamination

King Bio Inc. is recalling NET Remedies #25 Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

The agency’s classification

FDA (Drugs): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.

Plain-English summary

King Bio Inc. is recalling 190 bottles of NET Remedies #25 (Yellow, White and Purple Label) Homeopathic Preparation, Oral Liquid, 57 mL. The recall was initiated because the product is subject to microbial contamination.

The affected product is identified by Lot AUS-122017A with an expiration date of 12/19. The product was manufactured by King Bio Inc. in the U.S.A. and supplied by NET (Australia) Pty LTD. Distribution was nationwide in the U.S.A., as well as in Canada and Australia.

Consumers who have this product should stop using it and contact King Bio Inc. for further instructions or a refund.

The recalled product

Product
NET Remedies #25 (Yellow, White and Purple 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.
Affected units
190

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: AUS-122017A Exp. 12/19

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 →

Similar recalls