Medline recalls convenience kits with Huons Lidocaine Ampules due to FDA manufacturing quality issues. Affected kits include specific models and lot numbers. Consumers should contact Medline for details.
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
Medline is recalling convenience kits that contain Huons Lidocaine Ampules. The recall is due to quality issues found during an FDA inspection of Huons' manufacturing site. These kits are used for circumcision procedures and may pose a risk if the lidocaine ampules are not safe.
The recall is triggered by quality issues identified during an FDA inspection of Huons' manufacturing facility. This means the lidocaine ampules could be unsafe for medical use, potentially causing harm during circumcision procedures.
People who own or use Medline convenience kits with the specific model numbers and lot dates listed in the recall notice are affected. Those performing circumcision procedures using these kits are at the highest risk.
Check for model numbers CIT6780, CIT3225A, or CIT6325 on the kits. Look for lot numbers 2025102790, 2025102190, or 2025102390.
Identify the model number on the kit (CIT6780, CIT3225A, or CIT6325) to determine if it is affected.
Reach out to Medline Industries for specific instructions on how to return or replace the affected kits.
The recall is due to quality issues identified during an FDA inspection of Huons' manufacturing facility for the lidocaine ampules.
The affected models are CIT6780, CIT3225A, and CIT6325 with specific lot numbers listed in the recall notice.
Check the model number and lot number on the kit. Affected kits have model numbers CIT6780, CIT3225A, or CIT6325 and lot numbers 2025102790, 2025102190, or 2025102390.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2546-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2546-2026 from Medline. 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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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.
