{"url_path":"/fda/device/recalls/Z-2581-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIOGRAM PACK-LF\t\t  \tDYNJ21574J\t    JUDKINS PACK\t\t  \tDYNJ51126","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-02-27","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2581-2026%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":135,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2581-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-02-27\n**Report date:** 2026-07-01\n\n## Product\nConvenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIOGRAM PACK-LF\t\t  \tDYNJ21574J\t    JUDKINS PACK\t\t  \tDYNJ51126\n\n## Reason\nFirm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA.  Products not initially reported in RES 98601.\n\n## Affected lots\nDYNJ21574J   UDI-DI  10889942153497  Lots   21ALA586   21CLA398   21ELA408   21FLA144   21FLA788   21HLA420   21ILA431   DYNJ51126   UDI-DI  10889942122820  Lots   21ADA917\n\n## Distribution\nUS Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS,  KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI,  WY and the country of Barbados."}