{"url_path":"/fda/device/recalls/Z-2747-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-05","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2747-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medline Industries, LP"},"word_count":126,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2747-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-05\n**Report date:** 2026-07-29\n\n## Product\nMEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G\n\n## Reason\nMedline 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.\n\n## Affected lots\nUDI/DI 10198459280559 (each) 40198459280550 (case), Lot Number 25DBF430\n\n## Distribution\nUS:  OH, CA, IL, IN, FL, SC, AZ, NJ."}