Medline recalls LUMBAR PUNCTURE CHOICE kits (Model DYNDH1215) due to FDA-identified quality issues in Lidocaine Ampules. Affected units include specific lot numbers sold in 2025.
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 LUMBAR PUNCTURE CHOICE kits with model number DYNDH1:1215 because FDA found quality problems in the Lidocaine Ampules inside them. This recall is due to issues identified during a recent FDA inspection of the manufacturer's drug production facility.
The recall is triggered by FDA findings of quality issues during a manufacturing inspection of the drug production facility. This means the Lidocaine Ampules could have problems that affect their safety and effectiveness during medical procedures.
Healthcare professionals and medical facilities that purchased the LUMBAR PUNCTURE CHOICE kits with model number DYNDH1215 are likely affected. Patients receiving procedures using these kits may be at risk if the ampules are used without proper quality assurance.
Check for the model number DYNDH1215 on the Medline Convenience Kits. Affected units include specific lot numbers: 2025092390 (each) and 2025092390 (case).
Look for the model number DYNDH1215 and lot number 2025092390 on the kit packaging.
The FDA identified quality issues during a recent inspection of the manufacturer's drug production facility, leading to a recall of the Lidocaine Ampules in these kits.
The recall notice does not specify a remedy or action for affected units. Check the product details to confirm if it is affected.
The recall is due to quality issues identified by the FDA during a manufacturing inspection, but the specific safety risks are not detailed in the notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2544-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2544-2026 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.
