{"url_path":"/fda/device/recalls/Z-2275-2026","section_key":"summary","section_title":"DEVICE Recall: Oculus Technologies of Mexico, S.A. de C.V. — PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-27","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2275-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Oculus Technologies of Mexico, S.A. de C.V."},"word_count":128,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2275-2026\n\n**Recalling firm:** Oculus Technologies of Mexico, S.A. de C.V.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-27\n**Report date:** 2026-06-10\n\n## Product\nPhaseOne Antimicrobial Solution, Model/Catalog Number: 15050\n\n## Reason\nThe recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.\n\n## Affected lots\nUDI:00860009268616 Lot: 25G263\n\n## Distribution\nUS Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA."}