Medline recalls convenience kits with lidocaine ampules due to quality concerns found during FDA inspections. Affected kits include ART1145 and ART155A models from specific lot numbers. Consumers should check their kits for the listed model numbers and lot dates.
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 convenience kits that include lidocaine ampules because quality issues were found during an FDA inspection of the manufacturer's facility. These kits could pose risks if used improperly due to potential injection safety problems.
The lidocaine ampules in these kits were identified as having quality issues during an FDA inspection. This could lead to injection safety problems if the ampules are not properly manufactured or stored.
Healthcare professionals and medical facilities that use Medline convenience kits with lidocaine ampules are most at risk. The recall affects specific model numbers and lot dates.
Check for model numbers ART1145 or ART155A on the kits. Look for lot numbers 2025120590, 2025101490, or 2025100890 on the packaging.
Identify the model number (ART1145 or ART155A) and lot number (2025120590, 2025101490, or 2025100890) on the kit packaging.
The lidocaine ampules in these kits were found to have quality issues during an FDA inspection of the manufacturer's facility.
Model numbers ART1145 and ART155A are affected, with specific lot numbers listed in the recall notice.
No, the recall does not require immediate discontinuation; you can check the model and lot numbers to determine if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2533-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2533-2026 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.
