VitreQ recall: Sterility Concern
VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423
Why was VitreQ recalled?
Microscopic tears of the sterile pouch may compromise sterility
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?
All lots
- Product
- VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423
- Recalling firm
- Vitreq Bv
- Quantity
- N/A
- Distribution
- Nationwide
- Recall date
- February 5, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)