B. Braun Medical recalls CESK Northside Anesthesia Trays with model 555076 due to potential butyrate tubing cracking, making the product unusable. All units have been returned as of January 2026.
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.
B. Braun Medical is recalling CESK Northside Anesthesia Trays with model number 555076 because the butyrate tubing might crack, rendering the product unusable. This recall affects medical professionals who use these trays for anesthesia procedures.
The butyrate tubing (outside tube) in the anesthesia tray could crack, making the product unusable for medical procedures. This issue was identified by the manufacturer's supplier, Ferndale Laboratories, Inc.
Medical professionals who use CESK Northside Anesthesia Trays with model 555076 are affected. The risk is low as the product is no longer in circulation after all units were returned by January 2026.
Check for the model number 555076 on the tray. The product was distributed in January 2026 and all units have been returned by the manufacturer.
The manufacturer has confirmed all units were returned by January 2026, so no action is needed for current users.
No, all units were returned by January 2026 as per the manufacturer's notification.
The supplier identified potential cracking of the butyrate tubing, which makes the product unusable.
Look for the model number 555076 on the tray. The product was distributed in January 2026.
We’ve drafted a message you can send B. Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2263-2026 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall Z-2263-2026 from B. Braun Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
