King Bio Recalls Dr. King's SafeCare Rx Envious Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's SafeCare Rx Envious 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 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 per the rubric mandates a severity score of 5 (Critical) as it indicates a reasonable probability of serious adverse health consequences or death.
Plain-English summary
King Bio Inc. is recalling 16 bottles of Dr. King's SafeCare Rx Envious, 2 fl. oz. (59 mL), due to microbial contamination. The product is identified by Lot 041217D with an expiration date of 04/20, UPC 357955252023, and NDC 57955-2523-2.
The recalled product was distributed nationwide in the United States, as well as in Canada and Australia. The FDA has classified this recall as Class I, which indicates a reasonable probability that use of or exposure to the violative product will cause serious adverse health consequences or death.
Consumers who have this product should stop using it and contact King Bio Inc. for instructions on how to return the product or obtain a refund.
The recalled product
- Product
- Dr. King's SafeCare Rx Envious, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955252023, NDC 57955-2523-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Topical / Ophthalmic
- Hazard
- Affected units
- 16
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 (1)
- Lot: 041217D Exp. 04/20
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 →- CriticalKing Bio Recalls Dr. King's SafeCare Rx Calloused Due to Microbial Contamination
FDA (Drugs) · 2019-03-20
- SevereKing Bio Homeopathic Allergy Spray Recalled for Microbial Contamination
FDA (Drugs) · 2019-03-20
- CriticalKing Bio Recalls Heartburn Relief for Microbial Contamination
FDA (Drugs) · 2019-03-20
- SevereKing Bio Homeopathic Allergy Product Recalled for Microbial Contamination
FDA (Drugs) · 2019-03-20
- CriticalDr. King's Advanced Arnica Recalled for Microbial Contamination
FDA (Drugs) · 2019-03-20
Same hazard · microbial contamination
See all →- HighSV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination
FDA (Drugs) · 2026-10-07
- HighSV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination
FDA (Drugs) · 2026-10-07
- SevereMedline Ultrasound Breast Pack Recalled for Potential Sterility Breach
FDA (Devices) · 2026-09-09
- HighMedline Convenience Kits Recalled for Potential Sterility Breach
FDA (Devices) · 2026-09-09
- CriticalOptimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials
FDA (Drugs) · 2026-09-09
Similar recalls
- SevereDowning Labs Recalls B12 Injection Due to Sterility Assurance Concerns
FDA (Drugs) · 2015-11-25
- SevereDowning Labs Recalls Co-Enzyme Q-10 Injectable Due to Sterility Concerns
FDA (Drugs) · 2015-11-25
- SevereRed Mountain Compounding Recalls S-Vit B Complex Injection for Sterility Concerns
FDA (Drugs) · 2019-11-13
- SevereRed Mountain Compounding Recalls S-Hydroxocobalamin Injection Due to Sterility Concerns
FDA (Drugs) · 2019-11-13
- ModeratePfizer Recalls Oxecta Tablets Due to Failed Impurity Specifications
FDA (Drugs) · 2015-03-11
- HighMIC/B12 Injectable Vials Recalled for Lack of Sterility Assurance
FDA (Drugs) · 2022-09-21