{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99062",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US 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.",
      "recall_number": "Z-2591-2026",
      "product_description": "Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIO PACK\t  \tDYNJ30565C  \tDYNJ32555B  \t  ANGIO PACK-LF\t  \tDYNJ0774765U  \t  ANGIO TRAY\t  \tDYNJ46153A  \t  ANGIOGRAM TRAY\t  \tDYNJ33638K  \t  ANGIOGRAPHY DRAPE PK QVH-LF\t  \tDYNJ35110D  \t  ANGIOGRAPHY PACK\t  \tDYNJ44293D  \t  ANGIOGRAPHY PACK-LF\t  \tDYNJ0854485T  \tDYNJ35916J  \t  GENERAL ANGIO PACK\t  \tDYNJ57760B  \t  GENERAL ENDO PACK-LF\t  \tDYNJ0842873J  \t  JUDKINS PACK\t  \tDYNJ51126A  \t  RADIOLOGY ANGIO MAJOR PACK\t  \tDYNJ62858B  \t  TAVR JUDKINS PACK\t  \tDYNJ51127B",
      "product_quantity": "113,843 kits",
      "reason_for_recall": "Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA.  Products not initially reported in RES 98601.",
      "recall_initiation_date": "20260227",
      "center_classification_date": "20260625",
      "report_date": "20260701",
      "code_info": "DYNJ30565C    UDI-DI 10889942165704    Lots 21CDA555   21DDA970  DYNJ32555B    UDI-DI 10884389648216    Lot 21AMA053    DYNJ0774765U    UDI-DI 10193489634594    Lot 21FLA468    DYNJ46153A    UDI-DI 10889942185863    Lots 20XBH471   21BBC325    DYNJ33638K    UDI-DI 10193489343281    Lot 21HLA726    DYNJ35110D    UDI-DI 10193489329940    Lot 21IMC537    DYNJ44293D    UDI-DI 10193489833416    Lots 21CBE250   21CBX084   21FBB546   21HBD075   21KBN509   22ABV463   22BBX022   22DBJ641   22HBB710   22HBT960   22IBD236   22OBF392    DYNJ0854485T    UDI-DI 10193489864199    Lots 21FBC416   21GBL506   21IBO920   21JBS587  DYNJ35916J    UDI-DI 10193489838404    Lots 21CBF463   21DBP668   21DBR247    DYNJ57760B    UDI-DI 10193489342581    Lots 21CME104   21EME408   21FMD506   21GMG028   21JMF774   21KMH487    DYNJ0842873J    UDI-DI 10193489448917    Lots 21ADA204   21CDB566   21EDB709   21GDC532   21HDC041   21JDB401   21JDC566   21LDA726   22BDA893   22CDC138   22EDA075   22FDC040   22HDB149   22JDA080    DYNJ51126A    UDI-DI 10193489854886    Lots 21DDA694   21EDB249   21GDD164   21IDA472   21KDA815    DYNJ62858B    UDI-DI 10193489891263    Lots 21FMF601   21HMF637   21HMG835   21JMF531    DYNJ51127B    UDI-DI 10193489854893    Lot 22FBV791"
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}