The Recall Desk
Agency classClass IOur severity:CriticalFDA (Drugs)·D-0949-2019·Announced 2019-03-20

King Bio Recalls NET Remedies #20 Pain Relief Due to Microbial Contamination

King Bio Inc. is recalling NET Remedies #20 Pain Relief 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 FDA classified this recall as Class I, which corresponds to a Critical severity score of 5 according to the rubric.

Plain-English summary

King Bio Inc. is recalling NET Remedies #20 Pain Relief Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4213-2. The recall was initiated because the product is subject to microbial contamination. A total of 14,249 bottles are affected by this recall.

The affected product was distributed nationwide in the United States, as well as in Canada and Australia. Specific lot numbers and expiration dates are listed in the recall documentation, including lots expiring between September 2018 and June 2020.

Consumers who have this product should stop using it and contact King Bio Inc. for further instructions or a refund. The U.S. Food and Drug Administration (FDA) has classified this recall as Class I, indicating a reasonable probability that use of the product may cause serious adverse health consequences or death.

The recalled product

Product
NET Remedies #20 Pain Relief Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4213-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic Preparation
Hazard
Affected units
14,249

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 (15)

  • Lots: NR-010617M Exp. 01/20
  • NR-031516C Exp. 03/19
  • NR-061616L Exp. 06/19
  • NR-090115F Exp. 09/18
  • NR-090616M Exp. 09/19
  • NR-101416L Exp. 10/19
  • NR-120815C Exp. 12/18
  • NR-020118P Exp. 02/20
  • NR-022318K Exp. 02/20
  • NR-022318M Exp. 02/20
  • NR-052517A Exp. 05/20
  • NR-060517F Exp. 06/20
  • NR-060618A Exp. 06/20
  • NR-061418A Exp. 06/20
  • NR-121417B 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 →

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