FDA Drug recall D-0529-2026
Lidocaine HCl injection, USP, 1% 50mg/5mL (10 mg/mL), 5 mL Single Dose Vials, Rx only, Manufactured by: Huons Co, Ltd, Chungcheongbuk-do, K…
- FDA Drug
- Class II
- ongoing
- Published 2026-04-22
On 2026-04-22 the FDA classified a Class II recall of Lidocaine HCl injection, USP, 1% 50mg/5mL (10 mg/mL), 5 mL Single Dose Vials, Rx only, Manufactured by: Huons Co, Ltd, Chungcheongbuk-do, K… by Huons, citing lack of Assurance of Sterility.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0529-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-02 |
| Published | 2026-04-22 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Huons |
| Distribution | US |
Product
Lidocaine HCl injection, USP, 1% 50mg/5mL (10 mg/mL), 5 mL Single Dose Vials, Rx only, Manufactured by: Huons Co, Ltd, Chungcheongbuk-do, Korea NDC 73293-0001-1 (vial), NDC 73293-0001-2 (10 count carton); Distributed by: McKesson Corporation, dba Sky Packaging, NDC 63739-170-13 (vials), NDC 63739-170-24 (10 count cartons) and NDC 63739-170-27 (25 count cartons); Distributed by: Brookefield Pharmaceuticals, LLC, Brookefield, WI, Manufactured by: Huons Co., Ltd., 100 Bio valley-ro, Jecheon-si, Chungchengbuk-do, Korea, NDC 71351-021-05 (vials), NDC 71351-021-10 (10 count cartons), NDC 71351-021-25 (25 count cartons); Distributed by Novagenix Labs LLC, Morrisville, NC NDC 84769-0001-1 (vials), NDC 84769-0001-2 (10 count carton)
Reason
Lack of Assurance of Sterility
Identifiers
| ndc | 73293-0004-1 |
|---|---|
| ndc | 73293-0004-2 |
| ndc | 73293-0005-1 |
| ndc | 73293-0005-2 |
| ndc | 73293-0001-1 |
| ndc | 73293-0001-2 |
| ndc | 73293-0003-1 |
| ndc | 73293-0003-2 |
| ndc | 63739-170-13 |
| ndc | 63739-170-24 |
| ndc | 63739-170-27 |
| ndc | 71351-026-20 |
| ndc | 71351-026-25 |
| ndc | 71351-027-20 |
| ndc | 71351-027-25 |
| ndc | 71351-021-05 |
| ndc | 71351-021-10 |
| ndc | 71351-021-25 |
| ndc | 71351-023-05 |
| ndc | 71351-023-10 |
| ndc | 71351-023-25 |
| ndc | 84769-0001-1 |
| ndc | 84769-0001-2 |
| ndc | 84769-0002-1 |
| ndc | 84769-0002-2 |
| code_info | All lots within expiry |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0529-2026%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.