FDA Drug recall D-0739-2019
Dr. King's SafeCare Rx LymePlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006923, NDC 57955-…
- FDA Drug
- Class I
- terminated
- Published 2019-03-20
On 2019-03-20 the FDA classified a Class I recall of Dr. King's SafeCare Rx LymePlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006923, NDC 57955-… by King Bio, citing microbial contamination.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0739-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-07-20 |
| Published | 2019-03-20 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | King Bio |
| Distribution | US |
Product
Dr. King's SafeCare Rx LymePlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006923, NDC 57955-0069-2
Reason
Microbial contamination
Identifiers
| upc | 357955006923 |
|---|---|
| code_info | Lots: 072815F Exp. 07/18; 061716C Exp. 06/19; 020817D Exp. 02/20; 030518F Exp. 03/20 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0739-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.