The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0766-2019·Announced 2019-03-20

King Bio Recalls Dr. King's SafeCare Rx Allergies: Mold for Microbial Contamination

King Bio Inc. is recalling Dr. King's SafeCare Rx Allergies: Mold 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 minimum severity score of 4 per the rubric.

Plain-English summary

King Bio Inc. is recalling 1,329 bottles of Dr. King's SafeCare Rx Allergies: Mold, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The product is identified by NDC 57955-6501-2 and UPC 357955650126.

The affected lots are 072015D (Exp. 07/18), 022317F (Exp. 02/20), 123015B (Exp. 12/18), 062816B (Exp. 06/19), and 091616B (Exp. 09/19). The product was distributed nationwide in the U.S.A., 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
Dr. King's SafeCare Rx Allergies: Mold, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955650126, NDC 57955-6501-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic
Hazard
Affected units
1,329

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 (5)

  • Lots: 072015D Exp. 07/18
  • 022317F Exp. 02/20
  • 123015B Exp. 12/18
  • 062816B Exp. 06/19
  • 091616B Exp. 09/19

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 →

Related recalls

Same manufacturer · King Bio Inc.

See all →

Same hazard · microbial contamination

See all →

Similar recalls