Medline recalls two convenience kits with Lidocaine Ampules due to FDA-identified quality issues. Affected kits have specific model numbers and lot dates. 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 types of convenience kits that contain Lidocaine Ampules. The recall follows an FDA inspection finding quality issues with the ampules, which could pose risks if used improperly.
The Lidocaine Ampules were found to have quality issues during an FDA inspection of Huons Co., Ltd.'s manufacturing site. This could lead to improper injection if the ampules are not stable or contain incorrect medication.
People who own or use Medline Convenience Kits with the specified model numbers and lot dates are affected. Healthcare professionals using these kits for injections are most at risk.
Check for model numbers I550BF6C (lot 2025102290) or I505BF9C (lot 2025093090) on the Medline Convenience Kits. The kits contain Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules.
Identify the model number on your Medline Convenience Kit to see if it matches I550BF6C or I505BF9C.
Reach out to Medline Industries for specific instructions on what to do with the recalled kits.
The recall was issued by Huons Co., Ltd. due to quality issues identified during an FDA manufacturing inspection of their drug production facility.
The affected model numbers are I550BF6C (lot 2025102290) and I505BF9C (lot 2025093090).
The recall does not require immediate stop use; contact Medline for specific instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2538-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2538-2026 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.
