Medline recalls specific anterior hip kits containing Bupivacaine Hydrochloride in Dextrose Injection due to quality issues from the supplier. Affected kits have unique identifiers 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 specific anterior hip kits that contain Bupivacaine Hydrochloride in Dextrose Injection. This recall is due to quality issues identified by the supplier, which could affect the product's safety and effectiveness.
The recall is initiated by the supplier of the Bupivacaine Hydrochloride in Dextrose Injection due to quality issues. These issues could impact the product's safety and effectiveness when used in medical procedures.
Healthcare professionals using Medline's anterior hip kits with the specific SKU DYNJ909640G are likely affected. Those who have the kits with the listed lot numbers and UDI/DI identifiers are at risk.
Check for the SKU DYNJ909640G on the kit label. Look for the UDI/DI numbers 10198459280559 (each) and 40198459280550 (case), and the lot number 25DBF430.
Verify the SKU, UDI/DI numbers, and lot number on the kit to confirm if it is affected.
The supplier identified quality issues with the Bupivacaine Hydrochloride in Dextrose Injection, which is part of the Medline anterior hip kit.
The official recall notice does not specify a remedy or action steps for affected kits.
Check for the SKU DYNJ909640G, UDI/DI numbers 10198459280559 (each) and 40198459280550 (case), and lot number 25DBF430.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2747-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2747-2026 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.
