{
  "recall_number": "Z-1144-2022",
  "product_description": "Effluent Sample Bag",
  "company_name": "Baxter Healthcare Corporation",
  "reason": "Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.",
  "classification": "Class II",
  "status": "Terminated",
  "source": "Devices",
  "initiated_date": "2022-04-21T00:00:00.000Z",
  "slug": "effluent-sample-bag-z-1144-2022",
  "matched_lei": null,
  "updated_at": "2026-07-16T13:49:13.423Z"
}