Medline recalls anesthesia kits containing Huons Bupivacaine HCl in Dextrose Injection due to microbiology testing concerns and 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 anesthesia kits that contain Huons Bupivacaine HCl in Dextrose Injection. The recall is due to quality issues including microbiology testing data integrity problems and reported efficacy complaints. This could affect medical professionals using these kits for anesthesia procedures.
The recalled kits contain Bupivacaine HCl in Dextrose Injection that had microbiology testing data integrity concerns and reported efficacy complaints. This means the medication might not work as intended or could have quality issues that could affect patient safety during anesthesia procedures.
Medical professionals who own or use Medline anesthesia kits with the specified SKUs and lot numbers are most at risk. These kits are used for administering anesthesia during medical procedures.
Check for Medline kits labeled as 'ANESTHESIA TRAY' (SKU DYNJRA1355A) or 'SPINAL ANESTHESIA TRAY' (SKU DYNJRA2151). Look for specific lot numbers listed in the recall notice.
Identify your Medline anesthesia kit by SKU and lot number to confirm if it's affected.
Medline recalls these kits due to quality issues with the Bupivacaine HCl in Dextrose Injection, including microbiology testing data integrity concerns and reported efficacy complaints.
The recall notice does not specify a remedy or action for affected kits. Check the product details to confirm if it's affected.
Yes, affected kits have specific lot numbers listed in the recall: 26CBA272, 26ABS307, 25HBE663, 25FBA408, 25CBG043, 24FBT395 for SKU DYNJRA1355A, and 24FBT396 for SKU DYNJRA2151.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2231-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2231-2026 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.
