King Bio Recalls Homeopathic TMJ Formula Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic TMJ/Jaw Formula due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.
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 has classified this recall as Class I, which meets the rubric criteria for a Critical severity score.
Plain-English summary
King Bio Inc. is voluntarily recalling 2,368 bottles of Dr. King's Natural Medicine Homeopathic TMJ/Jaw Formula, 2 fl. oz. (59 mL). The recall is being conducted due to microbial contamination. The affected product is identified by NDC 57955-5032-2 and UPC 357955503224.
The recalled product was distributed nationwide in the United States, as well as in Canada and Australia. Specific lots affected include 060216C (Exp. 06/19), 070815A (Exp. 07/18), and 123016E (Exp. 12/19).
Consumers who have purchased this product should stop using it immediately and return it to the place of purchase for a refund. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product may cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic TMJ/Jaw Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503224, NDC 57955-5032-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 2,368
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: 060216C Exp. 06/19
- 070815A Exp. 07/18
- 123016E Exp. 12/19
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.
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