{"url_path":"/fda/device/recalls/Z-2675-2026","section_key":"summary","section_title":"DEVICE Recall: Wilcox Industries Corp. — The intended use is to be paired with a weapon for aiming purposes.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-06","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2675-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Wilcox Industries Corp."},"word_count":90,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2675-2026\n\n**Recalling firm:** Wilcox Industries Corp.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** FDA Mandated\n**Initiated:** 2026-04-06\n**Report date:** 2026-07-29\n\n## Product\nThe intended use is to be paired with a weapon for aiming purposes.\n\n## Reason\nWilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units should be returned to implement this change.\n\n## Affected lots\nNone provided.\n\n## Distribution\nUS Nationwide distribution in the state of NH."}