Skip to main content
Skip to recall details
Verified · FDAClass II — Possible RiskMedications

Lidocaine HCl injection, USP, 1% 50mg/5mL , 5 mL Single Dose Vials, Rx only Recall 2026

LIDOCAINE HYDROCHLORIDEIssued April 2, 2026Updated Reviewed by the Recall Watch editorial team

LIDOCAINE HYDROCHLORIDE 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 cart — recalled per FDA on 4/2/2026. Reason: Lack of Assurance of Sterility.

Agency
FDA
Issued
Apr 2, 2026
Brand
LIDOCAINE HYDROCHLORIDE
Distribution
1 states
Lots affected
1
What to do right now

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

Free case review

Were you or someone in your household prescribed this medication?

  • Free
  • No obligation
  • Licensed attorneys
Attorney advertising.Details

Recall Watch is not a law firm and does not provide legal or medical advice. Free case reviews are provided by independent licensed attorneys; Recall Watch may receive a referral fee. Prior results do not guarantee a similar outcome. Submitting this form does not create an attorney-client relationship. See our terms and privacy policy.

Verified summary of the official U.S. Food and Drug Administration notice · Issued April 2, 2026 · Last synced Nov 1, 2026

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 71351-021-25 (25 count cartons); Distributed by Novagenix Labs LLC, Morrisville, NC NDC 84769-0001-1 (vials), NDC 84769-0001-2 (10 count carton)

Available at AmazonAd
White first-aid box with bandages

Restock your medicine cabinet

First-aid kits, thermometers and OTC basics, searched on Amazon.

Shop at Amazon.com

Need it delivered? Start a free Amazon Prime trial.

Why it was recalled

Lack of Assurance of Sterility

Affected products & lot numbers
1 lot called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
All lots within expiry
Where was it sold
1 state

USA Nationwide.

nationwide
Official noticefda.gov
More recalls like this
7 related — by brand, contaminant, and category

Frequently asked questions

Is the LIDOCAINE HYDROCHLORIDE recall still active?

Yes, this recall is currently active as of April 2, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: All lots within expiry. Check the label on your product.

What should I do if I have the recalled LIDOCAINE HYDROCHLORIDE?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.