Z-2268-2026 Class II Ongoing
FDA device recall Z-2268-2026 was initiated by B Braun Medical Inc on January 29, 2026 and is designated Class II. Reason for recall: B. 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 t… The recall status is ongoing. Affected quantity: 690.
Recall Details
- Product Type
- Devices
- Report Date
- June 10, 2026
- Initiation Date
- January 29, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 690
Product Description
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
Reason for Recall
B. 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.
Distribution Pattern
US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.
Code Information
Lot Code: Model No 552126, UDI-DI (Primary Device) 04046955056903, UDI-DI (Unit Device ID) 04046955056897, Lot Number 0062031274