King Bio Recalls Dr. King's SafeCare Rx Environmental Adaptation Cold/Damp
King Bio Inc. is recalling 25 bottles of Dr. King's SafeCare Rx Environmental Adaptation Cold/Damp due to microbial contamination.
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 agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.
Plain-English summary
King Bio Inc. is recalling 25 bottles of Dr. King's SafeCare Rx Environmental Adaptation Cold/Damp, 2 fl. oz. (59 mL). The product is identified by NDC 57955-0284-2 and UPC 357955028420. The recall is due to microbial contamination.
The affected lots are 022316A (Exp. 02/19) and 031517A (Exp. 03/20). The product was distributed nationwide in the U.S.A., as well as in Canada and Australia.
Consumers should stop using the product and contact King Bio Inc. for further instructions.
The recalled product
- Product
- Dr. King's SafeCare Rx Environmental Adaptation Cold/Damp, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028420, NDC 57955-0284-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Herbal Supplement
- Hazard
- Affected units
- 25
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: 022316A Exp. 02/19
- 031517A Exp. 03/20
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
- SevereKingston Pharma Recalls Infant Cough Syrup Due to Microbial Contamination
FDA (Food) · 2019-05-08
- SevereZicam Cold Remedy Nasal Swabs Recalled for Microbiological Testing Failures
FDA (Drugs) · 2026-09-02
- ModerateOTC Nasal Decongestant Recalled Due to Manufacturing Process Deviation
FDA (Drugs) · 2024-01-10
- ModerateSafecor Recalls Acyclovir 400mg Tablets Due to Manufacturing Deviations
FDA (Drugs) · 2017-06-21
- SevereDowning Labs Recalls B12 Injection Due to Sterility Assurance Concerns
FDA (Drugs) · 2015-11-25
- SevereSafecor Health Recalls Doxycycline Tablets Due to Manufacturing Deviations
FDA (Drugs) · 2017-06-21