The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0744-2019·Announced 2019-03-20

King Bio Recalls Dr. King's SafeCare Rx Heart Regularity Circulation

King Bio Inc. is recalling Dr. King's SafeCare Rx Heart Regularity Circulation 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 per the rubric.

Plain-English summary

King Bio Inc. is recalling 386 bottles of Dr. King's SafeCare Rx Heart Regularity Circulation, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The product is identified by NDC 57955-0065-2 and UPC 357955006527.

The affected lots are 083115F (Exp. 08/18), 091516D (Exp. 09/19), and 020917K (Exp. 02/20). The product was distributed nationwide in the U.S.A., 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, it should be discarded or returned to the point of purchase.

The recalled product

Product
Dr. King's SafeCare Rx Heart Regularity Circulation, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006527, NDC 57955-0065-2
Manufacturer
King Bio Inc.
Category
Drug — Liquid Supplement
Hazard
Affected units
386

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: 083115F Exp. 08/18
  • 091516D Exp. 09/19
  • 020917K Exp. 02/20

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 →

Related recalls

Same manufacturer · King Bio Inc.

See all →

Same hazard · microbial contamination

See all →

Similar recalls