Fresenius Kabi Lidocaine HCl Injection Recall: Hair Found in Products

✎ GovInfoNow plain-language explainer

What happened, in plain English

Fresenius Kabi is recalling 25 single-dose vials of Lidocaine HCl Injection (2%) because hair was found in some products. This could cause injury if injected, so affected users should stop using the product.

Why it’s dangerous

Hair particles in the injection can cause injury when injected into the body. This is a contamination issue that could lead to adverse reactions or complications during medical procedures.

Who’s affected

Presumably healthcare professionals who use the product for medical injections. Patients receiving injections from this product are at risk if they have the recalled vials.

How to tell if you have this one

Check for the product name 'Lidocaine HCl Injection, USP, 2%', 25 single-dose vials, 5 mL per vial, with NDC Tray: 63323-208-05 and NDC Vial: 63323-208-01. The lot number is 6133801, expiring 01/2028.

Brand
Fresenius Kabi
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the NDC Tray number 63323-208-05 and NDC Vial number 63323-208-01 on the packaging.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates hair was found in some products, which could cause injury during injection. Do not use the recalled vials.

How can I check if I have the recalled product?

Check the NDC Tray number 63323-208-05 and NDC Vial number 63323-208-01 on the packaging. The lot number is 6133801, expiring 01/2028.

What should I do if I have the recalled product?

The recall does not specify a remedy, so contact Fresenius Kabi for further instructions.

Take action

Contact Fresenius Kabi

We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0726-2026 — Fresenius Kabi Fresenius Kabi

Hello,

I own a Fresenius Kabi that is covered by recall D-0726-2026 from Fresenius Kabi.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0726-2026 (July 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0726-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Fresenius Kabi USA, LLC recalls Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx only,

Lower-risk recall