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Medium risk Medical DevicesClass II

B. Braun CESK Harris Methodist Recall

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description

Updated January 29, 2026

B. Braun's CESK Harris Methodist adhesive component (model 555498) contains tubing that may crack during manufacturing, making it unusable. The defect was identified by the supplier of the Mastisol Liquid Adhesive component.

Is the B Braun Medical Inc recalled? Yes. This product was recalled by FDA on January 29, 2026. Details below.

What is recalled

B. Braun Medical Inc. CESK Harris Methodist, model/catalog number 555498, containing Mastisol Liquid Adhesive manufactured by Ferndale Laboratories, Inc.

Am I affected

You are affected if you have the CESK Harris Methodist device with model number 555498 from B. Braun Medical Inc.

What to do right now

Stop using this device. Contact B. Braun Medical Inc. or your supplier for return instructions and a replacement.

The hazard

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.

Brands affected

B Braun Medical Inc
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2266-2026
Classification
Class II
Recalled
January 29, 2026
Read the official notice

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