Medline recalls 10 types of convenience kits containing Huons Lidocaine Ampules due to FDA-identified quality issues from manufacturing inspections.
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 10 different convenience kits that include Huons Lidocaine HCL Injection ampules. The recall is because FDA inspections found quality problems with these ampules during manufacturing.
The recall is triggered by FDA inspections identifying quality issues with Huons Lidocaine HCL Injection ampules. These issues could potentially affect the safety and effectiveness of the medication during medical procedures.
Healthcare professionals using these kits for pain management or epidural procedures are most at risk. Patients receiving treatments with these kits could be affected if the ampules are used.
Check for model numbers PAIN0072L, PAIN1317, PAIN1579A, PAIN1885A, PAIN1967A, PAIN2269, PAIN2278, PAIN2305, PAIN2334, or SAMPA0147 on the kits. The lot numbers 25JDB100 through 25JLA942 are also associated with this recall.
Look for model numbers listed in the recall notice, such as PAIN0072L or PAIN1317.
Reach out to Medline Industries for assistance with the recall process.
The FDA identified quality issues with Huons Lidocaine HCL Injection ampules during a manufacturing inspection.
The affected models include PAIN0072L, PAIN1317, PAIN1579A, PAIN1885A, PAIN1967A, PAIN2269, PAIN2278, PAIN2305, PAIN2334, and SAMPA0147.
Check the model number on the kit and the lot number, which ranges from 25JDB100 to 25JLA942.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2534-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2534-2026 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.
