B. Braun Catheter Connectors Recalled for Leakage and Disconnection
B. Braun Medical is recalling specific catheter connectors because they may not stay closed, leading to 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 without reported injury.
Plain-English summary
B. Braun Medical, Inc. is recalling 1,020 units of SCNB4TK CONT STIM W/4 INCH INSUL TUOHY catheter connectors, Material Number 331756. These devices are used by physicians to provide a common access point for the delivery of anesthetics and fluids.
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 connectors has been observed. The affected units are from batches 61598215, 61602690, and 61610144.
The affected products were distributed nationwide in the United States as well as in Australia, Canada, Guatemala, and Kuwait. Healthcare providers and patients should stop using these specific connectors and contact B. Braun Medical for further instructions.
The recalled product
- Product
- SCNB4TK CONT STIM W/4 INCH INSUL TUOHY, Material Number 331756 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 conjunctio
- Manufacturer
- B. Braun Medical, Inc.
- Hazard
- Affected units
- 1,020
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 (3)
- Batch: 61598215
- 61602690
- 61610144
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.
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