VTI Bayonet Doppler recall: Sterility Concern
VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of…
Why was VTI Bayonet Doppler recalled?
Report of the product penetrating the sterile barrier; this could render the product unsterile.
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?
LOT NUMBER 11786-37683
- Product
- VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of…
- Recalling firm
- Vascular Technology, Inc.
- Quantity
- 25
- Distribution
- Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.
- Recall date
- July 16, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)