Medline recalls specific C-SECTION kits containing Bupivacaine Hydrochloride due to quality issues from Huons Co, Ltd. Affected kits have unique SKUs and lot numbers.
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.
Medline is recalling two specific C-SECTION convenience kits that contain Bupivacaine Hydrochloride. The recall is due to quality issues identified by the manufacturer Huons Co, Ltd., which has voluntarily recalled the product.
The recall is for quality issues with Bupivacaine Hydrochloride in Dextrose Injection, USP. Huons Co, Ltd. has issued a voluntary recall because of these issues, but the specific hazard mechanism isn't detailed in the notice.
Healthcare professionals using these kits for medical procedures are likely affected. The risk is highest for those handling the kits in clinical settings.
Check for Medline convenience kits labeled 'C-SECTION' with SKUs DYNJ910835 or DYNJ910835A. Lot numbers 25BBC541 or 25DBP805 are also indicators.
Identify the SKU and lot number on the kit to confirm if it's affected.
Huons Co, Ltd. has issued a voluntary recall due to quality issues with the Bupivacaine Hydrochloride in Dextrose Injection, USP.
The recall record does not specify a remedy or action steps for affected products.
Look for Medline kits labeled 'C-SECTION' with SKUs DYNJ910835 or DYNJ910835A and lot numbers 25BBC541 or 25DBP805.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2748-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2748-2026 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.
