EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT
Class I - DangerousWhat Should You Do?
- Check if you have this product: lots N5A0871KX N7A0527KX N7E0441KX N8J0039KX N8J0527KX N8J0820KX
- 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:
- Covidien LLC
- Reason for Recall:
- The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT
Product Codes/Lot Numbers:
lots N5A0871KX N7A0527KX N7E0441KX N8J0039KX N8J0527KX N8J0820KX
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1825-2019
Related Recalls
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