The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0944-2019·Announced 2019-03-20

King Bio Recalls NET Remedies #9 ER 911 Homeopathic Preparation

King Bio Inc. is recalling NET Remedies #9 ER 911 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 #9 ER 911 Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4209-2. The recall involves 38,399 bottles of the product.

The recall was initiated due to microbial contamination. The affected lots include NR-031816A, NR-073015F, NR-010617H, NR-011216C, NR-021717F, NR-050916A, NR-061716A, NR-080116B, NR-090115L, NR-090616H, NR-101916B, and NR-120815H.

The product was distributed nationwide in the United States, as well as in Canada and Australia. Consumers should stop using the product and contact King Bio Inc. for further instructions.

The recalled product

Product
NET Remedies #9 ER 911 Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4209-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic Preparation
Hazard
Affected units
38,399

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 (12)

  • Lots: NR-031816A Exp. 03/19
  • NR-073015F Exp. 07/18
  • NR-010617H Exp. 01/20
  • NR-011216C Exp. 01/19
  • NR-021717F Exp. 02/20
  • NR-050916A Exp. 10/19
  • NR-061716A Exp. 06/19
  • NR-080116B Exp. 08/19
  • NR-090115L Exp. 09/18
  • NR-090616H Exp. 09/19
  • NR-101916B Exp. 10/19
  • NR-120815H Exp. 12/18

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 →

Similar recalls