Stryker Neurovascular recall
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Why was Stryker Neurovascular recalled?
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
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: (01)00815742002386/Lot Number(s): 0000228865 0000370674
- Product
- Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
- Recalling firm
- Stryker, Inc.
- Quantity
- 11 units
- Distribution
- US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
- Recall date
- February 21, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)