B. Braun recalls CESK SHANDS Jackson 20055717 model 555884 due to potential butyrate tubing cracking, making it unusable. Affected units sold in 2023.
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 is recalling a specific medical device model because its butyrate tubing may crack, rendering it unusable. This affects patients using the device for medical purposes.
The butyrate tubing outside the device may crack, making the product unusable for medical purposes. This could lead to improper medical treatment if the device fails.
Patients using the CESK SHANDS Jackson 20055717 medical device are affected. Those with the specific model number 555884 are most at risk.
Check for the model number 555884 on the device. The product was sold in 2023 and is labeled as CESK SHANDS JACKSONVILLE 20055717.
Look for the model number 555884 on the device label.
The butyrate tubing may crack, rendering the product unusable for medical purposes.
Check the model number on the device; if it's 555884, contact B. Braun for further instructions.
The recall states the product may become unusable, but no specific injury risk is mentioned.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2269-2026 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2269-2026 from B. Braun. 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.
