Vortex MP Port Titanium Low Profile Implanted Port with recall
Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central venous placement (either…
Why was Vortex MP Port Titanium Low Profile Implanted Port with recalled?
Printed Instructions for Use (IFU) not shipped with device. The Instructions for Use contain the Warnings, Precautions, Contraindications, and Procedures for the Preparation, Implantation, and Post Operative Care of the implantable port, failure to follow the Instructions for Use may result in patient injury.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI-DI: 15051684018357 Lot Number: 5751582 Exp. Date: 31-Aug-2025
- Product
- Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central venous placement (either…
- Recalling firm
- Angiodynamics, Inc.
- Quantity
- 11 units
- Distribution
- US Nationwide distribution in the states of AZ, CA, DC, IN, PA.
- Recall date
- November 2, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)