{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Round Lake",
      "address_1": "Route 120 And Wilson Rd",
      "reason_for_recall": "Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints.  Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.",
      "address_2": "",
      "product_quantity": "3,255,096 total",
      "code_info": "Product Codes:  2C1071KJP, 2C1073KJP, 2C1075KJP    Lot Codes:  08J078  08K002  08K005  08K007  08K054  08K066  08M001  08M025  08M028  08M039  08N003  08N005  08N032  09A004  09A040  09A042  09A064  98025  98027  98028  98070  09(018  09C023  09(024  09C045  09C047  09(075  90029  90031  90033  90065  90069  90086  09E026  09E027  09E031  09F023  09F024  09F025  09F040  09F041  09F042  09G013  09G061  09G062  09H004  09H008  09H035  09H036  09H070  09H082  09J006  09J007  09J074  09J075  09K017  09K018  09K021  09K022  09K086  09K087  09M002  09M005  09M037  09M038  09M039  09M078  09N027  09N028  09N029  09N034  10A019  10A020  10A021  10A044  108010  108029  10C002  10C003  10C006  10C078  10C079  10C099  10C103  10C111  100026  100027  100028  100058  100062  100063  10E003  10E008  10E009  10E067  10G005  10G006  10G007  10G008  10G078  10G079  10H014  10H019  10H020  10H022  10H054  10H056  10H057  10H060  10H069  10H071  10H105  10H107  10J022  10J023  10J026  10J028  10J029  10J070  10J071  10J074  10K043  10K044  10K047  10K049  10K051  10K061  10K065  10K110  10M056  10M058  10M059  10M060  10N006  10N024  10N028  10N078  11A022  11A024  11A030  11A052  11A074  11A075  08K001  08K003  08K053  08K077  08M002  08N007  08N029  08N030  08N034  08N069  08N070  09A001  09A063  98026  98069  98071  09C046  90025  90032  90070  09E030  09F022  09F026  09G010  09H005  09H037  09J005  09J042  09J043  09J044  09J045  09J089  09K020  09K050  09M001  09M041  09N032  09N041  10A017  10A022  10A046  108014  108024  10C076  10C100  10C102  100025  100029  10E002  10E007  10E045  10E055  10G001  10G003  10G004  10H024  10H058  10H059  10H072  10J021  10J024  10J027  10J072  10K046  10K048  10K063  10K064  10M034  10M057  10N023  10N077  11A023  11A031  11A054  08K067  08M003  09A006  98078  90026  90085  09E052  09H001  09J071  09K053  09M003  09M077  108025  10C005  10C080  10C101  100059  10E053  10H023  10H106  10J030  10J045  10J069  10K066  10M086  10N027  11A025    Expiration Dates: 06/30/13, 12/31/13, 12/31/14, 06/30/14, 12/31/14, 06/30/15,12/31/15, 06/30/15",
      "center_classification_date": "20130627",
      "distribution_pattern": "Distributed Nationwide and in Puerto Rico.",
      "state": "IL",
      "product_description": "Brand Name: SV Elastomeric Infusion Device.    Indicated for the intravenous administration of medications.",
      "report_date": "20130703",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-1605-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65365",
      "termination_date": "20140604",
      "more_code_info": "",
      "recall_initiation_date": "20130607",
      "postal_code": "60073-9799",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}