B. Braun Contiplex Cont Nerve Block Connectors Recalled for Leakage
B. Braun Medical is recalling 108 Contiplex Cont Nerve Block 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 to patients, 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 108 units of the CNBFX350O Contiplex Cont Nerve Block connector (Material Number 331670, Batch 61602878). This connection device is used by physicians to provide a single access point to a catheter for the continuous administration of anesthetic 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. This defect could compromise the delivery of anesthetics.
The affected units were distributed nationwide in the United States and 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
- CNBFX350O CONTIPLEX CONT NERVE BLOCK, Material Number 331670 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
- Manufacturer
- B. Braun Medical, Inc.
- Hazard
- Affected units
- 108
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 (1)
- Batch: 61602878
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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