{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 8
    }
  },
  "results": [
    {
      "cfres_id": "220019",
      "product_res_number": "Z-2263-2026",
      "event_date_initiated": "2026-01-29",
      "event_date_posted": "2026-05-29",
      "recall_status": "Open, Classified",
      "res_event_number": "98862",
      "product_code": "OGE",
      "product_description": "Brand Name: B. BRAUN MEDICAL INC\nProduct Name: CESK NORTHSIDE ANESTHESIA TRAY\nModel/Catalog Number: 555076\nSoftware Version: N/A\nProduct Description: CESK NORTHSIDE ANESTHESIA TRAY\nComponent: No",
      "code_info": "Lot Code: Model No 555076, UDI-DI (Primary Device) 04046964313417, UDI-DI (Unit Device ID) 04046964313394, Lot Number 0062031523\n\nNote: In the original customer notification (JAN2026), 280 pieces were distributed, to date, all pieces have been returned.",
      "firm_fei_number": "2521402",
      "recalling_firm": "B Braun Medical Inc",
      "address_1": "824 12th Ave",
      "city": "Bethlehem",
      "state": "PA",
      "postal_code": "18018-3524",
      "additional_info_contact": "Allison Longenhagen\n001-484-2408373",
      "reason_for_recall": "B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of  MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.",
      "root_cause_description": "Process control",
      "action": "On January 29, 2026 and May 6, 2026 URGENT MEDICAL DEVICE RECALL letters were sent to customers to notify them of a recall of a kit component. Actions to be taken include to review inventory to identify affected product, discontinue use and segregate. Using the acknowledgement form, respond to B Braun who will send further instructions to return the product. Should there be any questions, comments, or concerns regarding the product you have received, please feel free to contact (844-903-6417) or recalls@bbraunusa.com;",
      "product_quantity": "280",
      "distribution_pattern": "US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.",
      "openfda": {
        "registration_number": [
          "1643817",
          "3004076349",
          "3035642068",
          "2029015",
          "3015173212",
          "2433012",
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          "8022210",
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        ],
        "fei_number": [
          "1000512168",
          "1643817",
          "1000138054",
          "3004076349",
          "3001236905",
          "3035642068",
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          "3045816907",
          "2521402",
          "3003737899",
          "1000160458",
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        ],
        "device_name": "Epidural Anesthesia Kit",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5120",
        "device_class": "2"
      }
    }
  ]
}