The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0950-2019·Announced 2019-03-20

King Bio Para Solve Homeopathic Liquid Recalled for Microbial Contamination

King Bio Inc. is recalling NET Remedies #6 Para Solve 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 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The FDA classified this recall as 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 score of 4 or higher.

Plain-English summary

King Bio Inc. is recalling NET Remedies #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2. The recall involves 11,489 bottles of the product. The reason for the recall is microbial contamination.

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 2018 and 2020.

Consumers should stop using the product and return it to the place of purchase for a refund or contact the manufacturer for further instructions.

The recalled product

Product
NET Remedies #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic
Hazard
Affected units
11,489

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 (16)

  • Lots: NR-031516H Exp. 03/19
  • NR-011216G Exp. 01/19
  • NR-021717C Exp. 02/20
  • NR-040417D Exp. 04/20
  • NR-061616E Exp. 06/19
  • NR-090115H Exp. 09/19
  • NR-090616E Exp. 09/19
  • NR-101416F Exp. 10/19
  • NR-120815L Exp. 12/18
  • NR-020118F Exp. 02/20
  • NR-022318F Exp. 02/20
  • NR-052218A Exp. 05/20
  • NR-071718G Exp. 07/20
  • NR-101117G Exp. 10/19
  • NR-120317F Exp. 02/19
  • NR-110117D Exp. 11/19

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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