Medline recalls 31 convenience kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules due to quality issues found during FDA inspection.
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 31 different convenience kits that include Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules. The recall is because these ampules were found to have quality issues during a recent FDA inspection of Huons Co., Ltd.'s manufacturing site.
The recall is triggered by quality issues identified during an FDA inspection of Huons Co., Ltd.'s manufacturing facility. The specific issue with the Lidocaine Ampules could potentially affect their safety or effectiveness, though the exact nature of the quality problem is not detailed in the recall notice.
Healthcare professionals and medical facilities that own or use the recalled Medline Convenience Kits are most at risk. The specific kits containing the affected Lidocaine Ampules are listed in the recall notice.
Check for the model numbers listed in the recall: SUT12260, MNS3390, MNS9715, ART351, P155615A, SUT18660A, MNS5985, DYNDL1351, ART600, SUT9710C, ID2060, SUT12265, DYNDH1466, SUT19665, P124863, ART352, DYNDH1699, and others. The kits were sold with specific lot numbers and UDI-DI codes as listed in the recall.
Identify if your Medline Convenience Kit has one of the listed model numbers (e.g., SUT12260, MNS3390) that includes the affected Lidocaine Ampules.
The recall is because Huons Co., Ltd. identified quality issues with the Lidocaine Ampules during an FDA manufacturing inspection of their facility.
The affected products are Medline Convenience Kits that contain Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules, with model numbers listed in the recall notice.
Check the model number and lot number on your kit. The recall lists specific model numbers and associated lot numbers that are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2542-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2542-2026 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.
