The Recall Desk
Agency classClass IOur severity:CriticalFDA (Drugs)·D-0829-2019·Announced 2019-03-20

King Bio Recalls Aller-Detox Herbicide Product Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's SafeCare Rx Aller-Detox: Herbicides & Pesticides 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 per the rubric mandates a severity score of 5 (Critical) due to the reasonable probability of serious adverse health consequences.

Plain-English summary

King Bio Inc. is recalling 586 bottles of Dr. King's SafeCare Rx Aller-Detox: Herbicides & Pesticides, 2 fl. oz. (59 mL). The recall was initiated due to microbial contamination. The affected product is identified by NDC 57955-2406-2 and UPC 357955240624.

The recalled product was distributed nationwide in the United States, as well as in Canada and Australia. The specific lots affected are 072115D (Expiration 07/18) and 060216B (Expiration 06/19).

Consumers should stop using the product and contact King Bio Inc. for further instructions or a refund. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product will cause serious adverse health consequences or death.

The recalled product

Product
Dr. King's SafeCare Rx Aller-Detox: Herbicides & Pesticides, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955240624, NDC 57955-2406-2
Manufacturer
King Bio Inc.
Category
Drug — Supplement
Hazard
Affected units
586

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 (2)

  • Lots: 072115D Exp. 07/18
  • 060216B Exp. 06/19

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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