King Bio Recalls Dr. King's SafeCare Rx Due to Microbial Contamination
King Bio Inc. is recalling 91 bottles of Dr. King's SafeCare Rx Stubborn & Contentious 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 voluntarily recalling 91 bottles of Dr. King's SafeCare Rx Stubborn & Contentious, 2 fl. oz. (59 mL). The recall is being conducted due to microbial contamination. The affected product is identified by NDC 57955-1031-2 and UPC 357955103028.
The recalled lots include 062316A (Exp. 06/19), 101716D (Exp. 10/19), and 122216D (Exp. 12/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.
Consumers should check their inventory for the specific lot numbers and expiration dates listed above. If the product is found, consumers should stop using it and contact King Bio Inc. for further instructions or a refund.
The recalled product
- Product
- Dr. King's SafeCare Rx Stubborn & Contentious, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955103028, NDC 57955-1031-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Veterinary Drug
- Hazard
- Affected units
- 91
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: 062316A Exp. 06/19
- 101716D Exp. 10/19
- 122216D 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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