Medline recalls two convenience kits containing Huons Lidocaine Ampules due to quality issues found during FDA inspections. Affected kits have specific model numbers and lot numbers. 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 Huons Lidocaine Ampules. The recall was initiated because the FDA found quality issues during an inspection of Huons' manufacturing facility.
The recall was triggered by quality issues identified during a recent FDA manufacturing inspection of Huons Co., Ltd.'s drug production site. The exact nature of the quality issues is not specified in the notice.
Healthcare professionals and medical facilities using the recalled convenience kits are most at risk. The recall affects specific model numbers and lot numbers of the kits.
Check for model numbers SM RADIOLOGY-ANGIO PACK-LF (DYNJ0621189X) or CONT (PAIN1470A) on the kits. Lot numbers 25ILA890, 25JLA514, or 25JDB583 are also associated with the affected units.
Reach out to Medline Industries for specific details about the recalled kits and instructions on how to return them.
The FDA identified quality issues during an inspection of Huons Co., Ltd.'s manufacturing facility, leading to a recall of the Lidocaine Ampules.
The affected model numbers are SM RADIOLOGY-ANGIO PACK-LF (DYNJ0621189X) and CONT (PAIN1470A).
Check the model number and lot number on the kit. Affected kits have specific lot numbers: 25ILA890, 25JLA514, or 25JDB583.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2537-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2537-2026 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.
