The Recall Desk
SevereFDA (Drugs)·D-0956-2019·Announced 2019-03-20

King Bio Recalls NET Remedies #8 Allergy Homeopathic Liquid Due to Microbial Contamination

King Bio Inc. is recalling NET Remedies #8 Allergy Homeopathic Preparation due to microbial contamination. The affected product was distributed in the U.S., Canada, and Australia.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that use of the product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a severity score of 4 (Severe) or higher.

Plain-English summary

King Bio Inc. is recalling NET Remedies #8 Allergy (Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4208-2. The recall is due to microbial contamination. The affected product was distributed nationwide in the U.S.A., as well as in Canada and Australia.

The recall covers 12,548 bottles. Specific lot numbers and expiration dates are listed in the official recall notice. Consumers should check their inventory for these specific lot numbers.

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

The recalled product

Product
NET Remedies #8 Allergy (Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4208-2
Manufacturer
King Bio Inc.
Affected units
12,548

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 (6)

  • Lots: NR-020618A Exp. 02/20
  • NR-051618E Exp. 05/20
  • NR-051818B Exp. 05/20
  • NR-101117D Exp. 10/19
  • NR-020118J Exp. 02/20
  • NR-092717B Exp. 09/19

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 →