Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model Number (UDI-DI): URF-P7 (04953170403811), URF-P7R (04953170403835), URF-V2 (04953170343582), URF-V2R (04953170343612), URF-V3 (04953170403385), URF-V3R (04953170403392).
- 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:
- Aizu Olympus Co., Ltd.
- Reason for Recall:
- Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.
Product Codes/Lot Numbers:
Model Number (UDI-DI): URF-P7 (04953170403811), URF-P7R (04953170403835), URF-V2 (04953170343582), URF-V2R (04953170343612), URF-V3 (04953170403385), URF-V3R (04953170403392).
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0348-2024
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