Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Single-pack UPN): M006L8406960
Class I - DangerousWhat Should You Do?
- Check if you have this product: GTIN: 08714729978718 Lot Numbers: 30261914, 30389513, 30429863, 30429864, 30479612 Exp. Date: 02-Oct-2025 to 3-Nov-2025
- 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.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Boston Scientific Corporation
- Reason for Recall:
- Manufactured with the incorrect component may result in lower power output and degradation or dimming of the aiming beam, leading to reduced efficiency of fiber performance. Continued use may cause overheating of the fiber connector, which could result in a burn, if touched
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Single-pack UPN): M006L8406960
Product Codes/Lot Numbers:
GTIN: 08714729978718 Lot Numbers: 30261914, 30389513, 30429863, 30429864, 30479612 Exp. Date: 02-Oct-2025 to 3-Nov-2025
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2233-2023
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