The Recall Desk
SevereFDA (Drugs)·D-0647-2019·Announced 2019-03-20

King Bio Recalls Homeopathic Caffeine Detox Due to Microbial Contamination

King Bio Inc. is recalling 19 bottles of Dr. King's Natural Medicine Homeopathic Caffeine Detox due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA 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 severity score of 4 or higher.

Plain-English summary

King Bio Inc. is recalling 19 bottles of Dr. King's Natural Medicine Homeopathic Caffeine Detox, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The product is identified by UPC 357955540229 and NDC 57955-6202-2.

The affected lots are 062415T with an expiration date of 06/18 and 092716B with an expiration date of 09/19. The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers who have this product should stop using it and contact King Bio Inc. for further instructions or a refund.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Caffeine Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955540229, NDC 57955-6202-2
Manufacturer
King Bio Inc.
Affected units
19

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: 062415T Exp. 06/18
  • 092716B 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 →