Medline recalls convenience kits containing Lidocaine injections due to FDA-identified quality issues at the manufacturer's facility. Affected kits have specific model numbers and lot codes.
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 injections because the manufacturer had quality problems found during a recent FDA inspection. This could affect users who have these kits for eye treatments.
The FDA found quality issues during a manufacturing inspection of the drug producer. This means the Lidocaine injections might not be safe for eye treatments, but the recall doesn't specify serious injury risks.
People who own or use Medline Ophthalmic Packs with Lidoc: 1) Model DYNJ57922A, 2) Lot numbers 25JLA852. Those with the kits for eye treatments are most at risk.
Check for the model number DYNJ57922A on the kit. Lot numbers 25JLA852 are also associated with this recall. The kits contain Lidocaine injections for eye use.
Look for model number DYNJ57922A and lot number 25JLA852 on the kit.
The FDA identified quality issues during a manufacturing inspection of the drug producer, so Medline is recalling these kits.
No, the recall doesn't require immediate stop use; the hazard is low risk and the remedy is to check product details.
Check the model number and lot number on the kit. If it matches DYNJ57922A and lot 25JLA852, contact Medline for details.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2547-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2547-2026 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.
