Reported Jun 10, 2026 · Ongoing
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model/Catalog Number: 552126 Software…
B Braun Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B Braun Medical Inc · 824 12th Ave · Bethlehem, PA · 18018-3524
Is this the product you have?
- Brand NameB. BRAUN MEDICAL INC
- Product NameCESK RIVERSIDE
- HEALTH SYSTEM Model/Catalog Number552126
- Software VersionN/A
- Product DescriptionCESK
- RIVERSIDE HEALTH SYSTEM ComponentNo
- Lot codes and dates
- Lot Code
Model No 552126UDI-DI (Primary Device) 04046955056903UDI-DI (Unit Device ID) 04046955056897Lot Number 0062031274
- Lot Code
- Amount recalled
- 690
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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