VIA Microcatheter VIA 21 recall: Labeling Error
VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the…
Why was VIA Microcatheter VIA 21 recalled?
Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.
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?
Catalog Number: VIA-21-154-01 UDI: (01)00842429101650(11)191104(17)221031(10)19110403M Lot Number: 19110403M
- Product
- VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the…
- Recalling firm
- MICROVENTION INC.
- Quantity
- N/A
- Distribution
- U.S. Nationwide distribution in the states of FL, IA, MI, MN, TN and TX.
- Recall date
- June 16, 2021
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)