Medline recalls two kits containing Huons Bupivacaine HCL in Dextrose Injection due to microbiology testing concerns and reported efficacy complaints. Affected kits have specific SKUs and lot numbers.
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
Medline is recalling two kits that contain Huons Bupivacaine HCL in Dextrose Injection. The recall is due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
The kits contain Bupivacaine HCL in Dextrose Injection that had microbiology testing data integrity concerns and reported efficacy complaints. This could affect the safety and effectiveness of the medication.
Healthcare professionals who use these kits for medical procedures are most at risk. The recall affects specific Medline kits with certain SKUs and lot numbers.
Check for Medline kits labeled as BLOCK TRAY (SKU DYNJRA1181C) or SPINAL BLOCK 25G WHTCRE 5S BU (SKU DYNJRA1860). Look for lot numbers 25DMF105, 25CMB575, or 24DMB099.
Identify the SKU and lot number on the kit to confirm if it is affected.
The recall is due to microbiology testing data integrity concerns and reported efficacy complaints with the Bupivacaine HCL in Dextrose Injection.
Medline kits labeled as BLOCK TRAY (SKU DYNJRA1181C) or SPINAL BLOCK 25G WHTCRE 5S BU (SKU DYNJRA1860) with lot numbers 25DMF105, 25CMB575, or 24DMB099.
The recall does not require immediate discontinuation; affected kits should be checked for the specific lot numbers and SKUs.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2234-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2234-2026 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.
