B. Braun Medical Recalls Catheter Connectors Due to 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 to patients, but the source text does not report 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 4,490 units of the NES1727KFX W /17GA TUOHY 19GA SPRW OT catheter connector (Material Number 333197). This connection device is used by physicians to provide a common access point to a catheter 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 identified by batch numbers 61587099, 61591814, 61603113, 61606091, 61615215, and 61618399.
The affected products were distributed nationwide in the United States and in Australia, Canada, Guatemala, and Kuwait. Healthcare providers and facilities should stop using the affected connectors and contact B. Braun Medical for instructions on return or replacement.
The recalled product
- Product
- NES1727KFX W /17GA TUOHY 19GA SPRW OT, Material Number 333197 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
- 4,490
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 (6)
- Batch: 61587099
- 61591814
- 61603113
- 61606091
- 61615215
- 61618399
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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