{"url_path":"/fda/device/recalls/Z-2268-2026","section_key":"summary","section_title":"DEVICE Recall: B Braun Medical Inc — Brand Name: B. BRAUN MEDICAL INC.  Product Name: CESK RIVERSIDE HEALTH SYSTEM  Model/Catalog Number: 552126  Software Version: N/A  Product Description: CESK RIVERSIDE HEALTH SYSTEM  Component: No","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-01-29","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2268-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"B Braun Medical Inc"},"word_count":128,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2268-2026\n\n**Recalling firm:** B Braun Medical Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-01-29\n**Report date:** 2026-06-10\n\n## Product\nBrand Name: B. BRAUN MEDICAL INC.  Product Name: CESK RIVERSIDE HEALTH SYSTEM  Model/Catalog Number: 552126  Software Version: N/A  Product Description: CESK RIVERSIDE HEALTH SYSTEM  Component: No\n\n## Reason\nB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of  MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.\n\n## Affected lots\nLot Code: Model No 552126, UDI-DI (Primary Device) 04046955056903, UDI-DI (Unit Device ID) 04046955056897, Lot Number 0062031274\n\n## Distribution\nUS Nationwide distribution in the states of AL, FL, PA, TX, VA, WA."}