Medline recalls Convenience Kits Block Tray Model DYNJRA1590 due to quality issues found during FDA inspection of Huons Co. Ltd.'s manufacturing site. Affected units contain Lidocaine Ampules with potential safety risks.
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 Block Tray Model DYNJRA15:90 because FDA inspections found quality issues with Lidocaine Ampules in these kits. This recall is important because the ampules could pose safety risks if used improperly.
The hazard comes from quality issues identified during FDA inspections of Huons Co. Ltd.'s manufacturing site. These issues could affect the safety and reliability of the Lidocaine Ampules in the kits.
Healthcare professionals and medical facilities that use Medline Convenience Kits Block Tray Model DYNJRA1590 are likely affected. Those handling the Lidocaine Ampules in these kits are at the highest risk.
Check for the model number DYNJRA1590 on the Medline Convenience Kits Block Tray. The lot number 25JLA522 and UDI-DI numbers 10193489284829 (each) and 40193489284820 (case) are also indicators of affected units.
Verify the model number DYNJRA1590 and lot number 25JLA522 on the kit to confirm it is affected.
The FDA identified quality issues during inspections of Huons Co. Ltd.'s manufacturing site, which could affect the safety of the Lidocaine Ampules in these kits.
The recall notice does not specify a remedy, so check the product details to confirm if it is affected and contact Medline for further instructions.
The recall is due to quality issues found during FDA inspections, but the specific safety risks are not detailed in the official notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2535-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2535-2026 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.
