B. Braun recalls ESPOCAN catheter connectors that may leak during use, posing a risk of disconnection. Affected units include specific batch numbers for medical devices used by physicians.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
B. Braun is recalling ESPO:1827QK ESPOCAN catheter connectors that may leak or disconnect during medical use. This could lead to improper administration of anesthetics or fluids, potentially causing harm to patients.
The catheter connectors may not stay closed during use, leading to leakage or disconnection of catheters. This can cause improper delivery of anesthetics or fluids, potentially harming patients during medical procedures.
Physicians using the ESPOCAN catheter connectors for medical procedures are most at risk. The recall affects specific batch numbers of the device used in hospitals and clinics.
Check for the model ES1827QK ESPOCAN with Material Number 333182. Affected units include batch numbers 61603106, 61610300, and 61619087.
Inspect the connector for signs of leakage or disconnection during use.
Reach out to B. Braun Medical Inc for specific guidance on affected units.
The model number is ES1827QK ESPOCAN with Material Number 333182.
Batch numbers 61603106, 61610300, and 61619087 are affected.
Check for the model ES1827QK ESPOCAN with Material Number 333182 and the specific batch numbers listed.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3390-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3390-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.