B. Braun recalls ESPOCAN Spinal/Epidural Trynrfit catheters (Catalog # 339114) due to filter membrane damage causing potential filter capacity issues. Affected units sold with specific lot numbers and UDI codes.
The filter capacity is not achieved due to damage of the filter membrane.
B. Braun is recalling ESPOCAN Spinal/Epidural Trynrfit catheters because the filter membrane can be damaged, which may lead to inadequate filter capacity. This could affect medical procedures by allowing contaminants to pass through the filter.
The filter membrane in the catheter can become damaged, which reduces the filter's ability to trap contaminants. This could allow particles or fluids to pass through the filter, potentially causing complications during medical procedures.
Healthcare professionals using the ESPOCAN Spinal/Epidural Trynrfit catheters for medical procedures are most at risk. Patients receiving these catheters during surgery or procedures may also be affected.
Check for the model ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT with catalog number 339114. Affected units have lot number 0061537250 and UDI code 04046964940613.
Verify the model number, catalog number, lot number, and UDI code to confirm if your catheter is affected.
The recall is for potential filter capacity issues due to filter membrane damage, but the risk is low as it does not cause immediate serious injury in normal use.
Check for the model ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT with catalog number 339114, lot number 0061537250, and UDI code 04046964940613.
The recall does not specify a remedy, so contact B. Braun Medical Inc for further instructions.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2466-2019 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2466-2019 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.
