Medline recalls spinal kits containing Huons Bupivacaine HCL in Dextrose Injection due to microbiology testing issues and efficacy complaints. Affected kits have specific SKUs and lot numbers listed in the recall notice.
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 surgery kits that contain Huons Bupivacaine HCL in Dextrose Injection. The product was recalled because of microbiology testing data integrity concerns and reported efficacy complaints. This could affect medical procedures if the injection is used improperly.
The bupivacaine injection was recalled due to concerns about microbiology testing data integrity and reported efficacy complaints. This means the product might not work as intended or could have contamination issues during medical procedures.
Healthcare professionals and patients who use these spinal surgery kits for procedures like spinal anesthesia. The risk is primarily for those administering the injection in medical settings.
Check for Medline spinal kits with specific SKUs: DYNJRA0245, DYNJRA0555, DYNJRA0836A, DYNJRA0978A, DYNJRA1034, DYNJRA9028, or DYNJRA9030. Look for lot numbers listed in the recall notice.
Identify your Medline spinal kit by SKU and lot number from the list provided in the recall notice.
The product was recalled due to microbiology testing data integrity concerns and reported efficacy complaints.
Check your Medline spinal kit's SKU and lot number against the list provided in the recall notice to see if it's affected.
The recall is due to quality issues, but the product does not pose an immediate risk of injury if used correctly. The hazard is related to potential product failure in medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2233-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2233-2026 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.
