Asheville, NC, United States
King Bio Inc. recalls
1 recall recorded since 2018, most recently on 20 July 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)1
Terminated Class I Drugs
- Recall started
- 20 July 2018
- Terminated
- 19 January 2022
- Reason
- Microbial contamination
- Distribution
- U.S.A. Nationwide, Canada, and Australia.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-0580-2019, D-0709-2019, D-0680-2019, D-0607-2019, D-0776-2019, D-0875-2019, D-0935-2019, D-0690-2019, D-0787-2019, D-0929-2019, D-0973-2019, D-0846-2019 and 453 more
- Dr. King's Natural Medicine Homeopathic Hydration, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955024224, NDC 57955-0242-2
- Dr. King's SafeCare Rx UlcerPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955175025, NDC 57955-0188-2
- Dr. King's SafeCare Rx Lonely Mind & Body High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955200024, NDC 57955-2001-2
- Dr. King's Natural Medicine Homeopathic Headache Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955515326, NDC 57955-5153-2
- Dr. King's SafeCare Rx CS-Breast, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021421, NDC 57955-0214-2
- Dr. King's SafeCare Rx Water Retention Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955027829, NDC 57955-0278-2
- NET Remedies #4 (Green Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
- Dr. King's SafeCare Rx Teething Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955001829, NDC 57955-0018-2
- and 457 more product lines
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.