Medline recalls L&D Continuous Epidural Trays (PAIN1699A) due to FDA-identified quality issues in Lidocaine Ampules. Affected units include specific model and lot numbers.
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 L&D Continuous Epidural Trays with model PAIN169:99A because the Lidocaine Ampules in them were flagged for quality problems during a recent FDA inspection. This recall affects healthcare providers using these kits for epidural procedures.
The recall is triggered by quality issues found in Lidocaine Ampules during an FDA inspection of Huons Co., Ltd.'s manufacturing site. These ampules are part of the Medline Convenience Kits used in epidural procedures.
Healthcare providers using the recalled L&D Continuous Epidural Trays for epidural procedures are most at risk. The recall specifically targets units with model PAIN1699A and lot numbers 25JLA719.
Check for model number PAIN1699A on the tray. Affected units have lot number 25JLA719 and are sold with specific UDI-DI numbers: 10195327411107 (single unit) and 40195327411108 (case).
Verify the model number (PAIN1699A) and lot number (25JLA719) on the tray to confirm if it's affected.
The FDA identified quality issues in the Lidocaine Ampules during an inspection of Huons Co., Ltd.'s manufacturing site.
Check the model number and lot number to confirm if it's affected; the recall does not specify a remedy.
The recall record does not specify a deadline for action.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2545-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2545-2026 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.
