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.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. 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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