Medline recalls two convenience kits due to quality issues with Lidocaine Ampules identified during FDA inspection. Affected kits include ART890B and IVS3350 models with specific 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 two convenience kits: the ARTERIAL LINE KIT (ART890B) and ULTRASOUND GUIDED IV SECUREMENT SET (IVS3350). The recall is due to quality issues with Lidocaine Ampules found during an FDA inspection of Huons Co., Ltd.'s manufacturing site.
The recall was initiated by Huons Co., Ltd. after FDA identified quality issues during their manufacturing inspection. The specific issue with the Lidocaine Ampules could affect medical safety during procedures.
Healthcare professionals using these kits for medical procedures are most at risk. The recall affects specific models and lot numbers sold by Medline.
Check for model numbers ART890B or IVS3350 on the kits. Lot numbers 2025102390 (ART890B) and 2025102490 (IVS3350) indicate affected units.
Identify the model number and lot number on the kit to confirm if it is affected.
Huons Co., Ltd. issued a recall notice for Lidocaine Ampules due to quality issues identified during an FDA manufacturing inspection.
The ARTERIAL LINE KIT (ART890B) and ULTRASOUND GUIDED IV SECUREMENT SET (IVS3350) with specific lot numbers are affected.
Check for model numbers ART890B or IVS3350 and lot numbers 2025102390 or 2025102490 on the kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2543-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2543-2026 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.
