FDAFDA · Food and drugs·Recall number Z-3370-2018
CE17TKPS CONTINUOUS EPIDURAL ANES TRAY, Material Number 332233 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.
Published October 10, 2018 · Recall initiated: July 20, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- B. Braun Medical, Inc.
- Distributor
- Worldwide Distribution: US (nationwide) and countries of: Australia, Canada, Guatemala and Kuwait.
- Lot
- Batch: 61582595, 61599648, 61605283, 61611124, 61614787
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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