CE17TKFCPS EPIDURAL FULL TRAY, Material Number 332078 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.
Reported: October 10, 2018 Initiated: July 20, 2018 #Z-3332-2018
Product Description
CE17TKFCPS EPIDURAL FULL TRAY, Material Number 332078 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.
Reason for Recall
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.
Details
- Recalling Firm
- B. Braun Medical, Inc.
- Units Affected
- 25020
- Distribution
- Worldwide Distribution: US (nationwide) and countries of: Australia, Canada, Guatemala and Kuwait.
- Location
- Allentown, PA
Frequently Asked Questions
What product was recalled? ▼
CE17TKFCPS EPIDURAL FULL TRAY, Material Number 332078 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.. Recalled by B. Braun Medical, Inc.. Units affected: 25020.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 10, 2018. Severity: Moderate. Recall number: Z-3332-2018.
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