Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EC20CS EPIDURAL CATHETER Recalled by B. Braun Medical, Inc. Due to The catheter connectors may not stay closed during...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B. Braun Medical, Inc. directly.
Affected Products
EC20CS EPIDURAL CATHETER, Material Number 333532 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.
Quantity: 2000
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B. Braun Medical, Inc.
B. Braun Medical, Inc. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report