{"url_path":"/fda/device/recalls/Z-2238-2026","section_key":"summary","section_title":"DEVICE Recall: Abiomed, Inc. — Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes.    1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA.     2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU.     3. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK.     4. Impella Controller, Packaged, US; Product Code: 004…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2011-01-17","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2238-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Abiomed, Inc."},"word_count":828,"has_tables":false,"body_markdown":null}