{"url_path":"/fda/device/recalls/Z-2584-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    DR G'S BREAST PACK\t  \tDYNJ51124B  \t  LIPO SUPPLEMENT PACK-LF\t  \tDYNJ0341174D  \t  PLASTIC PACK\t  \tDYNJ66746  \tDYNJ85702","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-2584-2026%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":146,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2584-2026\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.    DR G'S BREAST PACK\t  \tDYNJ51124B  \t  LIPO SUPPLEMENT PACK-LF\t  \tDYNJ0341174D  \t  PLASTIC PACK\t  \tDYNJ66746  \tDYNJ85702\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\nDYNJ51124B    UDI-DI 10193489579291    Lot 24ABS353    DYNJ0341174D    UDI-DI 10195327437749    Lot 24BBB383    DYNJ66746    UDI-DI 10193489375527    Lot 24BBD114  DYNJ85702    UDI-DI 10195327536213    Lot 24ABP053\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."}