The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0734-2019·Announced 2019-03-20

King Bio Recalls Dr. King's SafeCare Rx TUBR Miasm Due to Microbial Contamination

King Bio Inc. is recalling specific lots of Dr. King's SafeCare Rx TUBR Miasm 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 agency classification is FDA Class I, which mandates a severity score of at least 4 according to the rubric.

Plain-English summary

King Bio Inc. is voluntarily recalling 143 bottles of Dr. King's SafeCare Rx TUBR Miasm, 2 fl. oz. (59 mL), due to microbial contamination. The affected product is identified by NDC 57955-0304-2 and UPC 357955030423.

The recall covers specific lots with the following expiration dates: Lot 081815N (Exp. 08/18), Lot 080116D (Exp. 08/19), and Lot 012517L (Exp. 01/20). The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers should check their inventory for these specific lot numbers and expiration dates. If the product is found, consumers should stop using it and contact King Bio Inc. for further instructions or a refund.

The recalled product

Product
Dr. King's SafeCare Rx TUBR Miasm, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030423, NDC 57955-0304-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic
Hazard
Affected units
143

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 (3)

  • Lots: 081815N Exp. 08/18
  • 080116D Exp. 08/19
  • 012517L Exp. 01/20

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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