Medline recalls specific convenience kits containing lidocaine and bupivacaine due to quality issues found during FDA supplier inspection. Affected kits include models ACC010890 and DYNJ910066 series.
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
Medline is recalling convenience kits that contain lidocaine and bupivacaine injections because quality problems were found in the supplier's products during an FDA inspection. These kits are used for medical procedures and should be checked for the specific model numbers listed to determine if they are affected.
The recall is due to quality issues identified during a recent FDA inspection of the supplier. This means the injections could have manufacturing defects that might affect their effectiveness or safety, but there is no indication of immediate harm or injury.
Healthcare professionals and medical facilities that use these convenience kits for procedures like central line insertions. The risk is low as the issue relates to quality control during manufacturing, not immediate safety hazards.
Check for model numbers: ACC010890 (for drawer 6A adult central line) or DYNJ910066, DYNJ9855016V, and DYNJ9855016X. These kits were sold with specific lot numbers from 2024 to 2025.
Identify if your kit has model numbers ACC010890, DYNJ910066, DYNJ9855016V, or DYNJ9855016X.
Reach out to Medline Industries for confirmation of your specific kit's model and lot number to determine if it's affected.
The recall is due to quality issues identified during a recent FDA inspection of the supplier, which could affect the product's effectiveness or safety.
No, the recall is for quality control issues, not an immediate safety hazard. You can continue using them but should check if your specific model is affected.
Affected model numbers include ACC010890, DYNJ910066, DYNJ9855016V, and DYNJ9855016X, with specific lot numbers from 2024 to 2025.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2455-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2455-2026 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.
