Medline is recalling 52 different kits containing Huons Bupivacaine Hydrochloride in Dextrose Injection due to microbiology testing data integrity concerns and reported efficacy complaints.
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 52 specific kits that contain Huons Bupivacaine Hydrochloride in Dextrose Injection. The recall is due to microbiology testing data integrity issues and reported problems with the medication's effectiveness.
The recall is based on microbiology testing data integrity concerns and reported efficacy complaints. This means the medication may not be safe or effective for its intended use, potentially leading to adverse effects or treatment failures.
Healthcare professionals who use these kits for pain management or spinal anesthesia procedures are likely affected. Patients receiving these medications through these kits could be at risk if they have been exposed to the recalled products.
Check for Medline kits labeled as PAIN TRAY, SPINAL BLOCK TRAY, or SPINAL ANESTHESIA TRAY with specific SKUs listed in the recall notice. The kits have unique identifiers (UDI/DI numbers) and lot numbers as detailed in the recall.
Immediately stop using any Medline kits containing Huons Bupivacaine Hydrochloride in Dextrose Injection with the specified SKUs and lot numbers.
Medline is recalling 52 different kits containing Huons Bupivacaine Hydrochloride in Dextrose Injection, including PAIN TRAY, SPINAL BLOCK TRAY, and SPINAL ANESTHESIA TRAY kits with specific SKUs listed in the recall notice.
Check the product label for the specific Medline kit SKU and lot numbers listed in the recall notice. The recall includes 52 different kits with unique identifiers (UDI/DI numbers) and lot numbers.
Immediately stop using the product and contact Medline for instructions on how to return or dispose of the recalled kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2232-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2232-2026 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.
