AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Product code 5C9320. All serial numbers are affected for devices distributed from 02/11/2016 through 11/27/2018.
- 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:
- Baxter Healthcare Corporation
- Reason for Recall:
- Potential for the software on Automated PD System cyclers which can cause shortened dwell times during a Cycle-Based therapy
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
Product Codes/Lot Numbers:
Product code 5C9320. All serial numbers are affected for devices distributed from 02/11/2016 through 11/27/2018.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0849-2019
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