{"url_path":"/fda/device/recalls/Z-2399-2026","section_key":"summary","section_title":"DEVICE Recall: DT MedTech, LLC — Hintermann Series Talar Implant, Left, Size 2  REF 302112","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-24","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2399-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"DT MedTech, LLC"},"word_count":88,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2399-2026\n\n**Recalling firm:** DT MedTech, LLC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-24\n**Report date:** 2026-06-17\n\n## Product\nHintermann Series Talar Implant, Left, Size 2  REF 302112\n\n## Reason\nThrough customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.\n\n## Affected lots\nLot: AACAA/ DI: B095302112\n\n## Distribution\nWorldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR."}