Medline recalls two anesthesia kit models due to quality issues found during FDA supplier inspection. Affected kits contain lidocaine and bupivacaine injections. Consumers should check model numbers and lot numbers for affected items.
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 two specific anesthesia kit models because quality problems were found in the supplier's products during an FDA inspection. These kits include lidocaine and bupivacaine injections that could be unsafe if used.
The recall is due to quality issues identified during an FDA inspection of the supplier. The kits contain lidocaine hydrochloride injection and bupivacaine hydrochloride in dextrose injection, which were found to have problems during the inspection. However, no specific safety risks like injury or death are mentioned in the recall notice.
Healthcare professionals who use these anesthesia kits in medical settings are most at risk. Patients receiving procedures using these kits may also be affected.
Check for model numbers CV ANESTHESIA - ROOM SET UP with serial numbers starting with DYNJ905503F or DYNJ905503G. Lot numbers include 24GBR740, 24JBP984, 25ABJ069, and other specific codes listed in the recall notice.
Look for model numbers CV ANESTHESIA - ROOM SET UP on the kits to determine if they are affected.
Check the lot numbers listed in the recall notice (e.g., 24GBR740, 24JBP984) to confirm if your kit is affected.
The recall is due to quality issues identified during an FDA inspection of the supplier. The kits contain lidocaine hydrochloride injection and bupivacaine hydrochloride in dextrose injection that were found problematic.
Check the model numbers and lot numbers against the list provided in the recall notice to see if your kit is affected. If it is, you should stop using it and contact Medline for further instructions.
The recall notice states quality issues were found during an FDA inspection, but no specific safety risks like injury or death are mentioned. The hazard level is low risk.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2452-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2452-2026 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.
