Medline recalls two convenience kits due to quality issues found during FDA inspection of supplier. Kits contain Lidocaine and Bupivacaine injections that may not meet safety standards.
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 types of convenience kits because the supplier was found to have quality issues during an FDA inspection. These kits contain Lidocaine Hydrochloride and Bupivacaine Hydrochloride injections that could be unsafe.
The supplier was identified by the FDA as having quality issues during an inspection. This means the injections in the kits might not meet safety standards, but the recall does not specify immediate danger to users.
Healthcare professionals who use these kits for medical procedures are most at risk. The recall affects specific model numbers and lot numbers sold through Medline.
Check for model numbers ACC011142 or DYNJ8407. Look for lot numbers 26DDA462, 26DDA547, or 26DBB599 on the packaging.
Identify the model number and lot number on the packaging to confirm if it's affected.
The supplier was found to have quality issues during an FDA inspection, so the products were recalled to ensure safety standards are met.
Check the model number and lot number on the packaging to see if it's affected. If it is, contact Medline for further instructions.
The recall does not indicate immediate danger to users, but the products may not meet safety standards due to quality issues.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2454-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2454-2026 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.
