Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
β οΈ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Stryker, Inc.
- Reason for Recall:
- The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Product Codes/Lot Numbers:
UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1084-2024
Related Recalls
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.
Due to nonconforming products being inadvertently distributed.
Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.