Asclemed recalls Lidolog Kit (2% Lidocaine injection) due to label wrap covering barcode, making scanning difficult. Affected units have specific lot and expiration dates.
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Asclemed is recalling Lidolog Kit (2% lidocaine injection) because the label wrap covers the barcode, making it hard to scan. This issue doesn't pose a safety risk but could cause problems with product identification and prescription tracking.
The label wrap covers the barcode, which makes it difficult to scan the product. This could lead to identification issues but does not cause injury or health risks directly.
Prescription users of lidocaine injections who received this specific kit. Patients with the lot number 070126X1 and expiration date 12/31/2027 are most affected.
Check for the kit containing 2% lidocaine injection (2mL vial, single-use). Look for lot number 070126X1 and expiration date 12/31/2027 on the label.
Look for lot number 070126X1 and expiration date 12/31/2027 on the label.
No, the recall is due to labeling issues that affect scanning, not safety risks.
Check for lot number 070126X1 and expiration date 12/31/2027 on the label.
Check the label for the specific lot and expiration date. If it matches, contact your healthcare provider for guidance.
We’ve drafted a message you can send Asclemed to request your refund or repair — edit it as you like.
Subject: Recall D-0713-2026 — Asclemed Asclemed Hello, I own a Asclemed that is covered by recall D-0713-2026 from Asclemed. 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.
