Medline recalls spinal anesthesia 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 spinal anesthesia kits that contain Huons Bupivacaine HCL in Dextrose Injection. The kits were recalled because of quality issues including microbiology testing data integrity problems and reported efficacy complaints. This affects healthcare providers using these kits for spinal anesthesia procedures.
The recalled kits contain Huons Bupivacaine Hydrochloride in Dextrose Injection, which had quality issues including microbiology testing data integrity concerns and reported efficacy complaints. These issues could potentially affect the safety and effectiveness of the anesthesia.
Healthcare providers who use Medline spinal anesthesia kits containing Huons Bupivacaine HCL in Dextrose Injection are most at risk. These kits were distributed with specific SKUs and lot numbers listed in the recall.
Check if your Medline spinal anesthesia kit has a SKU number listed in the recall (e.g., DYNJRA1097, DYNJRA1154, etc.) and a lot number from the list provided in the recall notice.
Identify your Medline spinal anesthesia kit's SKU and lot number to confirm if it's affected by this recall.
Medline recalls these kits due to quality issues with Huons Bupivacaine Hydrochloride in Dextrose Injection, including microbiology testing data integrity concerns and reported efficacy complaints.
The affected kits include Medline spinal anesthesia kits with specific SKU numbers (e.g., DYNJRA1097, DYNJRA1154) and lot numbers listed in the recall notice.
No, the recall is for quality issues that do not pose an immediate risk of serious injury. You can continue using the kits but should check the recall list to confirm if your specific kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2236-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2236-2026 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.
