B. Braun recalls ES1827KDS spinal epidural kits with material number 333194 due to potential catheter connector leakage. Affected kits may leak or disconnect during use, risking infection or complications. Contact for return instructions.
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 spinal epidural kits that may leak or disconnect during use, potentially causing infections or complications. This is a safety issue for medical professionals using the kits.
The catheter connectors in these kits may not stay closed properly, leading to leakage or disconnection of catheters. This could cause infections or complications during medical procedures.
Physicians using the ES1827KDS spinal epidural kits with material number 333:194 are most at risk. The recall affects specific batch numbers sold for medical procedures.
Check for the model ES1827KDS and material number 333194 on the kit. Affected batches include 61592525, 61596331, 61601859, 61608500, 61611126, 61614295, 61618117, and 61621832.
Identify the model number (ES1827KDS) and material number (333194) on the kit.
Reach out to B. Braun Medical for specific return or repair instructions for affected batches.
The specific model number is ES1827KDS with material number 333194.
Affected batches are 61592525, 61596331, 61601859, 61608500, 61611126, 61614295, 61618117, and 61621832.
No, but you should check the batch number and contact B. Braun for instructions on next steps.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3393-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3393-2018 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.
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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.
