Atlas FDA

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model/Catalog Number: 552126 Software Versi

FDA device recall Z-2268-2026 · posted 2026-05-29 · Open, Classified

Recall details

Recalling firm
B Braun Medical Inc
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.
Action taken
On January 29, 2026 and May 6, 2026 URGENT MEDICAL DEVICE RECALL letters were sent to customers to notify them of a recall of a kit component. Actions to be taken include to review inventory to identify affected product, discontinue use and segregate. Using the acknowledgement form, respond to B Braun who will send further instructions to return the product. Should there be any questions, comments, or concerns regarding the product you have received, please feel free to contact (844-903-6417) or recalls@bbraunusa.com;
Root cause
Process control
Status
Open, Classified
Product code
OGE
Quantity affected
690
Distribution
US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.
Date initiated
2026-01-29
Date posted
2026-05-29
Location
Bethlehem, PA

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