Ce17tf Perifix FX Contin. Epidural SET recall
CE17TF PERIFIX FX CONTIN. EPIDURAL SET, Material Number 332234 Connection device used by physicians to provide various anesthetic and fluid…
Why was Ce17tf Perifix FX Contin. Epidural SET 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Batch: 61589584, 61617132, 61622878
- Product
- CE17TF PERIFIX FX CONTIN. EPIDURAL SET, Material Number 332234 Connection device used by physicians to provide various anesthetic and fluid…
- Recalling firm
- B. Braun Medical, Inc.
- Quantity
- 1032
- Distribution
- Worldwide Distribution: US (nationwide) and countries of: Australia, Canada, Guatemala and Kuwait.
- Recall date
- October 10, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)