{"url_path":"/fda/device/recalls/Z-2371-2026","section_key":"summary","section_title":"DEVICE Recall: ARROW INTERNATIONAL, LLC — Description/REF:  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1;  EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501;  EPIDURAL CATHETERIZATION KIT/AK-05502;  EPIDURAL CATHETERIZATION KIT/AK-05502D;  EPIDURAL CATHETERIZATION KIT/AK-05503;  EPIDURAL CATHETERIZATION KIT/AK-05503-L;  SPINAL ANES/EPIDURAL CATH KIT/AK-05560;  SPINAL ANES/EPIDURAL CATH KIT/ASK-0…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-21","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2371-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"ARROW INTERNATIONAL, LLC"},"word_count":1079,"has_tables":false,"body_markdown":null}