{"url_path":"/fda/device/recalls/Z-2748-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — MEDLINE convenience kits labeled as:    1) C-SECTION, Medline SKU DYNJ910835;   2) C-SECTION, Medline SKU DYNJ910835A; medical convenience kits","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-2748-2026%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":153,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2748-2026\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 convenience kits labeled as:    1) C-SECTION, Medline SKU DYNJ910835;   2) C-SECTION, Medline SKU DYNJ910835A; medical convenience kits\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\n1) Medline SKU DYNJ910835:  10198459152849 (each) 40198459152840 (case) Kit Lot Number 25BBC541;  2) Medline SKU DYNJ910835A: 10198459252570 (each) 40198459252571 (case), Kit Lot Number 25DBP805.\n\n## Distribution\nUS:  OH, CA, IL, IN, FL, SC, AZ, NJ."}