AV Fistula recall
AV FISTULA , Model No UTAV77T
Why was AV Fistula recalled?
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
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 00191072205179 Lots 961241 890241 70-051326 70-051979 70-053058
- Product
- AV FISTULA , Model No UTAV77T
- Recalling firm
- American Contract Systems Inc
- Quantity
- 90 kits
- Distribution
- US Nationwide distribution in the state of OH.
- Recall date
- March 26, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)