Lidocaine HCl injection recall
Huons Co., Ltd. recalled Lidocaine HCl injection on April 22, 2026 because of lack of Assurance of Sterility. It was sold nationwide.
Why it was recalled
Lack of Assurance of Sterility
What's recalled
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-…
Quantity: 33,599,925 ampules and 23658125 vials
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Huons Co., Ltd., Jecheon, N/A
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
USA Nationwide. - Status
- Ongoing
- Recall number
- D-0529-2026
- Source
- U.S. Food and Drug Administration
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