Medline recalls specific convenience kits containing Bupivacaine Hydrochloride in Dextrose Injection due to quality issues from Huons Co, Ltd. Affected kits have unique SKUs and lot numbers listed in the recall notice.
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 26 different convenience kits that contain Bupivacaine Hydrochloride in Dextrose Injection. The recall is due to quality issues with the product from Huons Co, Ltd., which was notified by B. Braun Medical Inc. The kits are used for medical procedures and should be checked for the specific SKUs and lot numbers listed in the recall.
The recall is due to quality issues with Bupivacaine Hydrochloride in Dextrose Injection, a product manufactured by Huons Co, Ltd. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC that this product has quality issues. The exact nature of the quality issue is not specified in the recall notice.
Medical professionals and patients who own or use the recalled Medline convenience kits containing Bupivacaine Hydrochloride in Dextrose Injection are affected. Those with the specific SKUs and lot numbers listed in the recall notice are at risk.
Check if your Medline convenience kit has one of the listed SKUs (e.g., DYKS1574A, DYNJ902378J) and the corresponding lot numbers (e.g., 25ELB079, 25IBN992) from the recall notice.
Verify your Medline convenience kit's SKU and lot number against the list provided in the recall notice to confirm if it is affected.
Huons Co, Ltd. has issued a voluntary recall of Bupivacaine Hydrochloride in Dextrose Injection due to quality issues, as notified by B. Braun Medical Inc.'s supplier, Spectra Medical Devices, LLC.
Check your kit's SKU and lot number against the list in the recall notice. If it matches, stop using it and contact Medline for further instructions.
The recall notice states there are quality issues with the product, but the exact risks are not specified.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2749-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2749-2026 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.
