Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm

Class I - Dangerous
🏥 Medical Devices Recalled: December 6, 2023 Stryker Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ 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.gov

FDA Recall Number: Z-1084-2024

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