Medline recalls spinal block 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 spinal block 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.
The recalled bupivacaine injection has quality issues that may affect microbiology testing data and product efficacy. This could lead to improper anesthesia delivery or infection risks.
Healthcare professionals using spinal anesthesia kits are most at risk. Patients receiving injections from these kits could be affected if the product is used.
Check for Medline kits labeled 'SPINAL BLOCK 22G QUINCKE 5S BU' with SKU DYNJRA9026. Lot numbers include 26BBD235, 26ABB534, 25DBT837, 25CBH118, 24FBT403, and 24FBJ505.
Verify the kit label and SKU to confirm if it matches the recalled items.
The recall is due to quality issues including microbiology testing data integrity concerns and reported efficacy complaints.
The official notice does not specify a remedy, so check the product details to confirm if it's affected.
Look for Medline kits labeled 'SPINAL BLOCK 22G QUINCKE 5S BU' with SKU DYNJRA9026 and specific lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2235-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2235-2026 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.
