The Recall Desk
HighFDA (Devices)·Z-3392-2018·Announced 2018-10-10

B. Braun Medical Recalls Espocan Spinal/Epid Trays Due to Leakage

B. Braun Medical is recalling 1,490 Espocan Spinal/Epid Trays because the catheter connectors may not stay closed, causing leakage or disconnection.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device with a functional defect (leakage/disconnection) that poses a risk of harm, but the source text does not report any specific injuries or illnesses, fitting the High severity criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

B. Braun Medical, Inc. is recalling 1,490 units of the Espocan Spinal/Epid Tray with 18G Tuohy, Material Number 333193. This connection device is used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for the delivery of anesthetics.

The recall was initiated because the catheter connectors may not stay closed during use. In some cases, leakage or disconnection of the catheters from the catheter connectors has been observed. The affected batches are 61597447, 61605030, 61609257, 61613551, and 61618397.

The product was distributed nationwide in the United States and in Australia, Canada, Guatemala, and Kuwait. Healthcare providers should stop using the affected trays and contact B. Braun Medical for further instructions.

The recalled product

Product
ESPOCAN SPINAL/EPID TRAY W/ 18G TUOHY, Material Number 333193 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
Affected units
1,490

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (5)

  • Batch: 61597447
  • 61605030
  • 61609257
  • 61613551
  • 61618397

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 93 recalled by B. Braun Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 93 products in this recall →